US1870858A - Method for the production of ethylene glycols and ethylene hydrocarbons - Google Patents
Method for the production of ethylene glycols and ethylene hydrocarbons Download PDFInfo
- Publication number
- US1870858A US1870858A US400164A US40016429A US1870858A US 1870858 A US1870858 A US 1870858A US 400164 A US400164 A US 400164A US 40016429 A US40016429 A US 40016429A US 1870858 A US1870858 A US 1870858A
- Authority
- US
- United States
- Prior art keywords
- aluminum
- zinc
- ethylene
- amalgam
- production
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 title description 7
- 238000000034 method Methods 0.000 title description 5
- 239000005977 Ethylene Substances 0.000 title description 3
- -1 ethylene hydrocarbons Chemical class 0.000 title description 3
- 229930195733 hydrocarbon Natural products 0.000 title description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 22
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 17
- 229910052725 zinc Inorganic materials 0.000 description 17
- 239000011701 zinc Substances 0.000 description 17
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 16
- 229910052782 aluminium Inorganic materials 0.000 description 16
- 229910052751 metal Inorganic materials 0.000 description 15
- 229910000497 Amalgam Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 9
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 description 9
- 239000000047 product Substances 0.000 description 7
- 239000003153 chemical reaction reagent Substances 0.000 description 6
- 150000002576 ketones Chemical class 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
- 229910000761 Aluminium amalgam Inorganic materials 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 229910052793 cadmium Inorganic materials 0.000 description 3
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- UERBIJRDJNPTJD-UHFFFAOYSA-N aluminum mercury Chemical compound [Al].[Hg] UERBIJRDJNPTJD-UHFFFAOYSA-N 0.000 description 1
- FJMNNXLGOUYVHO-UHFFFAOYSA-N aluminum zinc Chemical compound [Al].[Zn] FJMNNXLGOUYVHO-UHFFFAOYSA-N 0.000 description 1
- 238000005267 amalgamation Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229960002523 mercuric chloride Drugs 0.000 description 1
- 150000002730 mercury Chemical class 0.000 description 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000003698 tetramethyl group Chemical class [H]C([H])([H])* 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/18—Polyhydroxylic acyclic alcohols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/18—Polyhydroxylic acyclic alcohols
- C07C31/20—Dihydroxylic alcohols
Definitions
- the present invention relates to the production of homologues of ethylene glycol and ethylene hydrocarbons, and to the production of pinacone from acetone. More particularly the invention relates to the activation of an aluminum reagent by the formation of a thin'layer of an active amalgam upon the surface of the aluminum.
- the introduction of a third metal into the amalgam greatly increases the activity therereactions which are impossible with -alumi
- the metal introduced into the ordinary aluminum-mercury amalgam is preferably zinc.
- amalgams may be conducted by the use of soluble salts ofmercury and of the third metal, these salts being precipitated upon aluminum which is immersed or suspended in the solution of these salts.
- Another 'method of forming the amalgam of this invention is to melt the aluminum and third metal together thus forming an alloy which may then be ground to any desired degree and subsequently amalgamated on its surface by treatment with the mercury salts.
- glycolates according to the following general reaction If the glycolate thus ob'tained be treated With water, a' glycol and aluminum hydroxide are obtained: l
- the above equations describe reactions which take place in a non-aqueousmedium.- If'water be introduced into the reacting mi); ture, nascent hydrogen is evolved. This tetr amethyl' nascent hydrogen will lead to the formation of a series of reduction products; Under such conditions ketones will produce secondaryalcohols ornooern+an;ornxnaor-rcnn
- the improved activated aluminum reagent may be prepared by amalgamating an alloy of aluminum and another metal,.preferably zinc. In this instance the amalgam is prepared-according to the standard practiceof forming mercury amalgams of metals.
- Afmalgams made with mercury and purealuminum are subject tothe disadvantagevv that the layer of amalgam is rather easily de-. tached during the reaction and frequently the reaction stops as the result of this.
- T 1 zinc present in the amalgam layer a viscous tacky material is formed in which, the zinc may act as a cementing substance to keep the aluminum and mercury together.
- the advantage gained by the present invention is that any kind ofaluminum may be employed, and thealuminum may be used .in the form of filings or even in the iform of rough shavings. Moreover it has been the experience of organic chemists that not all makes of pure aluminum may be employed in carrying out these catalytic reactions. Indeed it is the general experience that there is but one kind of aluminum a product made in Germany which'will yield pinacone as the product of the reaction of acetone. By practicing the present invention, however, any kind of aluminum may beemployed and even better results obtained than with the above mentioned foreign product.
- the percent-age of zinc present in the alloy may be varied withinwide limits, depending upon the product desired. For the production of pinacone the percentage of zinc is figured to metallic zinc.
- the step of treating said ketones protect by Letters Patwith an aluminum amalgam containing" a small percentage of a metallic element selectedfrom the. group consisting of zinc and cadmium.
- zinc chloride will analyze a little less than possessesthe advantage thatanytype of aluminum can be employed and that it is not
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
.. No Drawing. Original application filed May 18, 1926, Seria1 No. 109,961, now Patent No. 1,752,0l6, dated March 25, 1930.v Divided and this application filed. October 16,- 1929. seriai'umeooaoi latentecl Aug. 9, 1932 res v PATENT" OFFNJE;
ALEXANDER T. MAXIMOIF, or "vnnonnnr, ITALY, ASSIGNOR TO Eli-IE neuea'rucx CHEMICAL COMPANY; v NECTICUT OF NAUG-ATUGK, CONNECTICUT, A CORPORATION OF CON?- M THOD FOR THE PRODUCTION or ETVHYLENE eLYooLs Ann ETI-IYLENE :ezrnnocannoivs I l This case is a division of my application Serial No. 109,961, filed May 18, 1926, now Patent No. 1,7 52,016, issued March 25, 1930.
The present invention relates to the production of homologues of ethylene glycol and ethylene hydrocarbons, and to the production of pinacone from acetone. More particularly the invention relates to the activation of an aluminum reagent by the formation of a thin'layer of an active amalgam upon the surface of the aluminum.-
The ordinary method of amalgamating aluminum for use in the reduction of organic num activated by th usual methods.
compounds does not impart to it suflicierit' activity. According to the present invention the introduction of a third metal into the amalgam greatly increases the activity therereactions which are impossible with -alumi The metal introduced into the ordinary aluminum-mercury amalgam is preferably zinc.
b Other metals, such; as cadmium may also be employed. While the invention is not limited to any particular method of forming the reagent, the following may serve asillustrations. The amalgam may be conducted by the use of soluble salts ofmercury and of the third metal, these salts being precipitated upon aluminum which is immersed or suspended in the solution of these salts. Another 'method of forming the amalgam of this invention is to melt the aluminum and third metal together thus forming an alloy which may then be ground to any desired degree and subsequently amalgamated on its surface by treatment with the mercury salts.
lVhen acetone and other ketones and derivatives thereof are treated with the improved reagent it will be found that the nature of the reaction is dependent upon the amount of third metal present in the amalgam.
hen ketones are treated with aluminum,
num glycolates according to the following general reaction If the glycolate thus ob'tained be treated With water, a' glycol and aluminum hydroxide are obtained: l
lVhen acetone is treated with the improved reagent the end product will-be ethylenevglycol or pinacol. v 1
If the amount of third metal be increased to from 7 to 30% by weight of the aluminum,
ethylene hydrocarbons are produced when ketones are treated. For example acetone will yield propylene: i 3CH ;CO.CH +2Al= l v v The above equations describe reactions which take place in a non-aqueousmedium.- If'water be introduced into the reacting mi); ture, nascent hydrogen is evolved. This tetr amethyl' nascent hydrogen will lead to the formation of a series of reduction products; Under such conditions ketones will produce secondaryalcohols ornooern+an;ornxnaor-rcnn The improved activated aluminum reagent may be prepared by amalgamating an alloy of aluminum and another metal,.preferably zinc. In this instance the amalgam is prepared-according to the standard practiceof forming mercury amalgams of metals.
Afmalgams made with mercury and purealuminum are subject tothe disadvantagevv that the layer of amalgam is rather easily de-. tached during the reaction and frequently the reaction stops as the result of this. With T 1 zinc present in the amalgam layer a viscous tacky material is formed in which, the zinc may act as a cementing substance to keep the aluminum and mercury together. By increasing the percentage of zinc, say up to in the aluminum zinc alloy, a large percentage of propylene will appear in the reaction when acetone is used as the starting material. Vhen an alloy contains 7%01 zinc, propylene continues to appear in large quantities in this reaction. When the amount of zinc is reduced to 2% or less, very little propylene will appear, and pinacone is obtained as the main product. a
The same results may be obtained by'using mixtures of zinc and mercuric salts with aluminum inthe preparation of the amalgam.
For instance if amalgamation of the aluminum 'is carried out by using a solution of 5% oflzinc chloride and 10% mercuric chloride,
the treatment of acetone with such amalgamated aluminum. yields pinacone in large quantities, and relatively free; from propylene and other products. I
The advantage gained by the present invention is that any kind ofaluminum may be employed, and thealuminum may be used .in the form of filings or even in the iform of rough shavings. Moreover it has been the experience of organic chemists that not all makes of pure aluminum may be employed in carrying out these catalytic reactions. Indeed it is the general experience that there is but one kind of aluminum a product made in Germany which'will yield pinacone as the product of the reaction of acetone. By practicing the present invention, however, any kind of aluminum may beemployed and even better results obtained than with the above mentioned foreign product. The percent-age of zinc present in the alloy may be varied withinwide limits, depending upon the product desired. For the production of pinacone the percentage of zinc is figured to metallic zinc. If a zinc compound is employed, calculations' are made accordingly. For example serve as illustrations of some of the uses to which the improved aluminum amalgam may be put. It will be understood, however that the reagent may be variously employed in reduction reactions in the presence of water, as well as in reactions where the aluminum forms a compound with all or part of the reacting material. The claims are therefore to. be interpreted broadly. The expres sions metallic element, metal and zinc as used in the claims, are descriptive of these materials as single elements, or where, they are available as such for the purpose of the invention, and the percentages given in'the claims refer to percentages of the metal, not
ofits salt. It is to be understood therefore that salts of zinc and the other metals which may beemployed are comprehended by the claims.
Having thus described my invention, what I claim and desire to ent' is: r
In the production of ethylene glycols from ketones, the step of treating said ketones protect by Letters Patwith an aluminum amalgam containing" a small percentage of a metallic element selectedfrom the. group consisting of zinc and cadmium.
2. In the production of pinacone from acetone, the step of treating said acetone with an aluminum amalgam containing not more than approximately 3% of a third metallic element selected from the group consistin of zinc and cadmium.
a 8. n the production of pinacone from acetone, the step of treating said acetone with an aluminum amalgam containing not more than approximately 3% of zinc, said zinc having the properties of increasing the reactivity of the amalgam, and holding the components of the amalgam together.
Signed at Milan, Italy, this 27th day of September, 1929.
ALEXANDER T. MAXIMOFF.
zinc chloride: will analyze a little less than possessesthe advantage thatanytype of aluminum can be employed and that it is not
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US400164A US1870858A (en) | 1926-05-18 | 1929-10-16 | Method for the production of ethylene glycols and ethylene hydrocarbons |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US109961A US1752016A (en) | 1926-05-18 | 1926-05-18 | Catalyst for the production of ethylene glycols and ethylene hydrocarbons |
| US400164A US1870858A (en) | 1926-05-18 | 1929-10-16 | Method for the production of ethylene glycols and ethylene hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1870858A true US1870858A (en) | 1932-08-09 |
Family
ID=26807562
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US400164A Expired - Lifetime US1870858A (en) | 1926-05-18 | 1929-10-16 | Method for the production of ethylene glycols and ethylene hydrocarbons |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1870858A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4336148A (en) * | 1977-09-07 | 1982-06-22 | Ciba-Geigy Corporation | Complex compound, process for their preparation, and their use |
-
1929
- 1929-10-16 US US400164A patent/US1870858A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4336148A (en) * | 1977-09-07 | 1982-06-22 | Ciba-Geigy Corporation | Complex compound, process for their preparation, and their use |
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