GB506473A - A process for obtaining organic oxy-compounds - Google Patents
A process for obtaining organic oxy-compoundsInfo
- Publication number
- GB506473A GB506473A GB22079/38A GB2207938A GB506473A GB 506473 A GB506473 A GB 506473A GB 22079/38 A GB22079/38 A GB 22079/38A GB 2207938 A GB2207938 A GB 2207938A GB 506473 A GB506473 A GB 506473A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phase
- compounds
- acid
- oxy
- esters
- 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
- 238000000034 method Methods 0.000 title abstract 3
- 239000012071 phase Substances 0.000 abstract 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- 150000002148 esters Chemical class 0.000 abstract 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- 239000004215 Carbon black (E152) Substances 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- 229930195733 hydrocarbon Natural products 0.000 abstract 3
- 150000002430 hydrocarbons Chemical class 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 150000001735 carboxylic acids Chemical class 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- -1 acetic acid Chemical class 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 229940072049 amyl acetate Drugs 0.000 abstract 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 238000006266 etherification reaction Methods 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 238000000605 extraction Methods 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 abstract 1
- 230000036571 hydration Effects 0.000 abstract 1
- 238000006703 hydration reaction Methods 0.000 abstract 1
- 230000002209 hydrophobic effect Effects 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 150000002894 organic compounds Chemical class 0.000 abstract 1
- 239000003208 petroleum Substances 0.000 abstract 1
- 150000007519 polyprotic acids Polymers 0.000 abstract 1
- 230000001737 promoting effect Effects 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 238000011084 recovery Methods 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid group Chemical group C(CCC(=O)O)(=O)O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- HVZJRWJGKQPSFL-UHFFFAOYSA-N tert-Amyl methyl ether Chemical class CCC(C)(C)OC HVZJRWJGKQPSFL-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
506,473. Separating organic compounds. NAAMLOOZE VENNOOTSCHAP DE BATAAFSCHE PETROLEUM MAATSCHAPPIJ. July 25, 1938, No. 22079. Convention date, Aug. 10, 1937. [Class 2 (iii)] Organic oxy-compounds such as alcohols, ethers and esters arc obtained from mixtures comprising two liquid phases encountered in the course of manufacturing such oxy-compounds, by separating the phases and extracting at least a part of the oxy-compound from the phase of more hydrophobic character, such as a hydrocarbon phase, by contacting it with a part of the other phase at a temperature below that prevailing during the pbase separation. The process may be used for the removal of free carboxylic acid, such as acetic acid, from the ester phase of a mixture consisting of an ester phase, such as an amyl acetate phase obtained from amylene and acetic acid, and an esterification catalyst phase, such as a sulphuric acid phase, or to obtain an alcohol from the hydrocarbon phase of an alcoholcontaining mixture consisting of an olefinecontaining hydrocarbon phase and an olefine hydration catalyst acid phase, such as an inorganic polybasic acid phase, or to obtain an alcohol from the ether phase of an alcoholcontaining mixture consisting of an ether phase and an etherification catalyst phase. The extractor used may be a tower for promoting counter-current contact or a mixing tank and the extraction may be carried out continuously, batchwise or intermittently. Typical esters which may be freed from the corresponding free carboxylic acid are the ethyl, propyl, butyl, amyl and allyl esters of formic, propionic, butyric, crotonic, benzoic, succinic and methacrylic acids or esters containing halogen or hydroxy substituents. The process may also be applied to the recovery of methyl alcohol in the production of methyl-tertiary amyl ethers from a tertiary amylene-pentane fraction and methyl alcohol.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US506473XA | 1937-08-10 | 1937-08-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB506473A true GB506473A (en) | 1939-05-30 |
Family
ID=21966508
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB22079/38A Expired GB506473A (en) | 1937-08-10 | 1938-07-25 | A process for obtaining organic oxy-compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB506473A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0175443A3 (en) * | 1984-09-17 | 1986-07-02 | Exxon Research And Engineering Company | Improved alcohol recovery process |
| EP0219229A1 (en) * | 1985-09-16 | 1987-04-22 | Exxon Research And Engineering Company | Improved process for recovery of alcohols from acid streams |
-
1938
- 1938-07-25 GB GB22079/38A patent/GB506473A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0175443A3 (en) * | 1984-09-17 | 1986-07-02 | Exxon Research And Engineering Company | Improved alcohol recovery process |
| EP0219229A1 (en) * | 1985-09-16 | 1987-04-22 | Exxon Research And Engineering Company | Improved process for recovery of alcohols from acid streams |
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