GB601817A - Process for making salts of carboxylic acids - Google Patents
Process for making salts of carboxylic acidsInfo
- Publication number
- GB601817A GB601817A GB2429145A GB2429145A GB601817A GB 601817 A GB601817 A GB 601817A GB 2429145 A GB2429145 A GB 2429145A GB 2429145 A GB2429145 A GB 2429145A GB 601817 A GB601817 A GB 601817A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cadmium
- oxide
- acid
- ethylene
- sodium hydroxide
- 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
Links
- 150000003839 salts Chemical class 0.000 title abstract 4
- 150000001735 carboxylic acids Chemical class 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 11
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 abstract 9
- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 abstract 9
- 235000019441 ethanol Nutrition 0.000 abstract 9
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 6
- 238000010438 heat treatment Methods 0.000 abstract 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Substances OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 5
- -1 propyl alcohols Chemical class 0.000 abstract 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 abstract 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 4
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 3
- 229910052793 cadmium Inorganic materials 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 239000000047 product Substances 0.000 abstract 3
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 abstract 3
- 229910052708 sodium Inorganic materials 0.000 abstract 3
- 239000011734 sodium Substances 0.000 abstract 3
- 235000011149 sulphuric acid Nutrition 0.000 abstract 3
- 229960001124 trientine Drugs 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- 229910001868 water Inorganic materials 0.000 abstract 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 abstract 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 2
- YZGQDNOIGFBYKF-UHFFFAOYSA-N Ethoxyacetic acid Chemical compound CCOCC(O)=O YZGQDNOIGFBYKF-UHFFFAOYSA-N 0.000 abstract 2
- 239000004471 Glycine Substances 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 150000001414 amino alcohols Chemical class 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 238000001914 filtration Methods 0.000 abstract 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 abstract 2
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 abstract 2
- 239000011707 mineral Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- 239000001117 sulphuric acid Substances 0.000 abstract 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 1
- GVNHOISKXMSMPX-UHFFFAOYSA-N 2-[butyl(2-hydroxyethyl)amino]ethanol Chemical class CCCCN(CCO)CCO GVNHOISKXMSMPX-UHFFFAOYSA-N 0.000 abstract 1
- WXOFXOLJVGPQHX-UHFFFAOYSA-N C=C.C=C.C=C.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O Chemical group C=C.C=C.C=C.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O WXOFXOLJVGPQHX-UHFFFAOYSA-N 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- 229910000881 Cu alloy Inorganic materials 0.000 abstract 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 abstract 1
- MNYVCPNTOOUBJE-UHFFFAOYSA-N NCCNCCN.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O Chemical compound NCCNCCN.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O MNYVCPNTOOUBJE-UHFFFAOYSA-N 0.000 abstract 1
- DRHKHYAIVWMBAS-UHFFFAOYSA-N NCCNCCNCCN.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O Chemical compound NCCNCCNCCN.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O.C(C)O DRHKHYAIVWMBAS-UHFFFAOYSA-N 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- 235000021355 Stearic acid Nutrition 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 150000001447 alkali salts Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 239000012043 crude product Substances 0.000 abstract 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 239000000706 filtrate Substances 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 235000011167 hydrochloric acid Nutrition 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000004310 lactic acid Substances 0.000 abstract 1
- 235000014655 lactic acid Nutrition 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- KFIGICHILYTCJF-UHFFFAOYSA-N n'-methylethane-1,2-diamine Chemical compound CNCCN KFIGICHILYTCJF-UHFFFAOYSA-N 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 1
- 235000006408 oxalic acid Nutrition 0.000 abstract 1
- 150000002913 oxalic acids Chemical class 0.000 abstract 1
- 230000020477 pH reduction Effects 0.000 abstract 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 229920000151 polyglycol Polymers 0.000 abstract 1
- 239000010695 polyglycol Substances 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 125000000075 primary alcohol group Chemical group 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- 239000010935 stainless steel Substances 0.000 abstract 1
- 229910001220 stainless steel Inorganic materials 0.000 abstract 1
- 239000008117 stearic acid Substances 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
- C07F1/005—Compounds containing elements of Groups 1 or 11 of the Periodic Table without C-Metal linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Salts of carboxylic acids are prepared by heating an alcohol containing a primary alcohol group with an alkali metal hydroxide in the presence of a cadmium catalyst at a temperature sufficiently elevated to cause liberation of hydrogen from the reaction mixture. The salts may be converted to the free acids by treating with mineral acid. It is stated that the invention may be applied to the process of oxidising amino alcohols described in Specification 601,816. The alcohols used contain a hydroxyl group attached to a terminal carbon atom which may be attached to a saturated or unsaturated straight or branched chain aliphatic radical or to a carbocyclic or heterocyclic radical, e.g. methyl, ethyl, propyl alcohols and higher alkanols having up to twenty or more carbon atoms; glycols and polyglycols of the ethylene and propylene glycol series; benzyl, phenyl ethyl and cinnamyl alcohols and amino alcohols having more than one carbon atom. The cadmium catalyst may be cadmium metal or a compound of the metal such as the oxide and fresh portions of catalyst may be added during the reaction. The temperature employed is generally 140 DEG to 300 DEG C. and atmospheric or elevated pressure may be employed. The reaction vessel is preferably formed of or lined with copper or copper alloys or with cadmium or may be of stainless steel. In examples: (1) and (2) glycine is obtained by heating monoethanolamine, potassium hydroxide and cadmium oxide, washing and filtering the crude product, evaporating the filtrate to dryness, extracting with ethyl alcohol followed by filtration of the extract and acidification with acetic acid; (3) tetraethanol ethylene diamine is heated with sodium hydroxide, water and cadmium oxide under hydrogen pressure and the sodium salt of tetracarboxymethyl ethylene diamine produced may be converted to the free acid by means of strong mineral acids such as sulphuric or hydrochloric acids; (4) potassium tetracarboxymethyl ethylene diamine is made by heating tetraethanol ethylene diamine, aqueous potassium hydroxide and cadmium oxide; (5) sodium tetracarboxymethyl propylene diamine is made by heating tetraethanol propylene diamine, aqueous sodium hydroxide and cadmium oxide; (6) pentaethanol diethyllene triamine is heated with aqueous sodium hydroxide and cadmium oxide to produce sodium pentacarboxymethyl diethylene triamine; (7) sodium hexacarboxymethyl triethylene tetramine is obtained by heating hexaethanol triethylene tetramine, aqueous sodium hydroxide and cadmium oxide; (8) n-hexanol, aqueous sodium hydroxide, cadmium oxide and stearic acid are heated and after distilling the product to recover unreacted hexanol the residue is treated with sulphuric acid to obtain caproic acid; (9) butyric acid is obtained by heating n-butanol, aqueous sodium hydroxide and cadmium oxide and acidifying the product as in (8); (10) beta-ethoxy ethyl alcohol, sodium hydroxide, water and cadmium oxide are heated under hydrogen pressure, the unreacted alcohol is removed by distillation and the residue acidified with sulphuric acid to yield ethoxy acetic acid. Other products specified are the alkali salts of carboxylic acids such as glycollic and oxalic acids from ethylene glycol, lactic acid from propylene glycol, dicarboxymethyl amine from diethanolamine, tricarboxymethyl amine from triethanolamine and isopropyl and butyl dicarboxymethyl amines from the corresponding isopropyl and butyl diethanolamines. Comparative results obtained in catalysed and uncatalysed reactions for the preparation of glycine and of salts of tetracarboxy methyl ethylene diamine are tabulated. Tetraethanol ethylene diamine is made by reaction of ethylene diamine and ethylene oxide. Tetraethanol-propylene diamine iss prepared by reacting ethylene oxide with a mixture of propylene diamine, water and ethanol and distilling the reaction mixture under reduced pressure. Penta-ethanol-diethylene-triamine and hexaethanol-triethylene-tetramine are made by reacting ethylene oxide with a mixture of ethanol and diethylene triamine and triethylene-tetramine respectively.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB601817A true GB601817A (en) | 1948-05-13 |
Family
ID=1738252
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2429145A Expired GB601817A (en) | 1945-09-19 | Process for making salts of carboxylic acids |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB601817A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3062719A (en) * | 1959-10-19 | 1962-11-06 | Geigy Chem Corp | Trisodium calcium diethylenetriaminepentaacetic acid, compositions containing the same, and the use thereof |
| US3404179A (en) * | 1964-03-13 | 1968-10-01 | Electro Chimie Metal | Process for preparing adipic acids by alkaline fusion of e-hydroxy-caproic acid and its derivatives |
| JPS5228774B1 (en) * | 1970-12-26 | 1977-07-28 | ||
| US4810426A (en) * | 1986-01-28 | 1989-03-07 | Monsanto Company | Process for making glyphosate from n-phosphonomethyl-2-oxazolidone |
-
1945
- 1945-09-19 GB GB2429145A patent/GB601817A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3062719A (en) * | 1959-10-19 | 1962-11-06 | Geigy Chem Corp | Trisodium calcium diethylenetriaminepentaacetic acid, compositions containing the same, and the use thereof |
| US3404179A (en) * | 1964-03-13 | 1968-10-01 | Electro Chimie Metal | Process for preparing adipic acids by alkaline fusion of e-hydroxy-caproic acid and its derivatives |
| JPS5228774B1 (en) * | 1970-12-26 | 1977-07-28 | ||
| US4810426A (en) * | 1986-01-28 | 1989-03-07 | Monsanto Company | Process for making glyphosate from n-phosphonomethyl-2-oxazolidone |
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