FR2245591B1 - - Google Patents
Info
- Publication number
- FR2245591B1 FR2245591B1 FR7425342A FR7425342A FR2245591B1 FR 2245591 B1 FR2245591 B1 FR 2245591B1 FR 7425342 A FR7425342 A FR 7425342A FR 7425342 A FR7425342 A FR 7425342A FR 2245591 B1 FR2245591 B1 FR 2245591B1
- Authority
- FR
- France
- Prior art keywords
- organic acid
- butanol
- solution
- isobutene
- acid
- 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
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
- C07C29/03—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
- C07C29/04—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
-
- 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
- C07C31/02—Monohydroxylic acyclic alcohols
- C07C31/12—Monohydroxylic acyclic alcohols containing four carbon atoms
Abstract
1443106 t-Butanol MITSUBISHI RAYON CO Ltd 11 June 1974 [25 July 1973 7 March 1974] 25883/74 Heading C2C t-Butanol is obtained by reacting isobutene with water at 20-120‹ C. in the presence of a strong acid ion-exchange resin and an organic acid under conditions such that the liquid product obtained is a homogeneous solution. In a preferred embodiment, (1) isobutene or a hydrocarbon mixture containing it reacts with an aqueous organic acid solution in the presence of the resin, (2) unaltered hydrocarbons are removed by distillation, (3) the residual mixture is distilled to give a mixture (A) consisting mainly of t-butanol and organic acid ester thereof, and an aqueous organic acid solution (B), (4) A, with if necessary further water, is treated with acid resin to hydrolyse the ester, (5) the hydrolysed product is separated into an aqueous t-butanol solution (C) and an aqueous organic acid solution (D), and (6) D is recycled to step 1. In an example, step 1 is carried out in two reactors, the first of a complete mixing type and the second of plug flow type. The organic acid is preferably a C 1 -C 6 saturated aliphatic acid (e.g. acetic or propionic acid). Isobutene may be reacted selectively in the presence of other hydrocarbons, e.g. n-butenes and butanes.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8371973A JPS5622855B2 (en) | 1973-07-25 | 1973-07-25 | |
JP2649174A JPS5314044B2 (en) | 1974-03-07 | 1974-03-07 | |
BE1006146A BE819255A (en) | 1973-07-25 | 1974-08-28 | METHOD OF MANUFACTURING TERTIO-BUTYL ALCOHOL |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2245591A1 FR2245591A1 (en) | 1975-04-25 |
FR2245591B1 true FR2245591B1 (en) | 1978-11-24 |
Family
ID=27159525
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7425342A Expired FR2245591B1 (en) | 1973-07-25 | 1974-07-22 |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE819255A (en) |
CA (1) | CA1029750A (en) |
DE (1) | DE2430470A1 (en) |
FR (1) | FR2245591B1 (en) |
GB (1) | GB1443106A (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6051451B2 (en) * | 1978-11-06 | 1985-11-14 | 三菱レイヨン株式会社 | Manufacturing method of tertiary butyl alcohol |
JPS6058893B2 (en) | 1979-04-27 | 1985-12-23 | 東亜燃料工業株式会社 | Method for producing tertiary alcohol |
JPS6058894B2 (en) | 1979-06-26 | 1985-12-23 | 東亜燃料工業株式会社 | Manufacturing method of tertiary alcohol |
DE3027478A1 (en) * | 1980-07-19 | 1982-03-04 | Ruhrchemie Ag, 4200 Oberhausen | METHOD FOR PRODUCING DIMETHYLBENZYLCARBINOL AND DIMETHYLBENZYLCARBINYLFORMIAT |
DE3029739A1 (en) * | 1980-08-06 | 1982-09-16 | Toa Nenryo Kogyo K.K., Tokyo | Tertiary alcohol prepn. - by reacting iso-olefin or hydrocarbon mixt. contg. iso-olefin with water in the presence of a catalyst |
JPS6059217B2 (en) * | 1980-12-25 | 1985-12-24 | 東亜燃料工業株式会社 | Method for producing secondary alcohol |
US4443383A (en) * | 1981-03-19 | 1984-04-17 | Rohm And Haas Company | Preparation of methacrolein and methacrylonitrile from tert-butyl alkanoates |
GB8322574D0 (en) * | 1983-08-23 | 1983-09-28 | Humphreys & Glasgow Ltd | Mixed alcohols |
DE3628008C1 (en) * | 1986-08-19 | 1987-11-05 | Deutsche Texaco Ag, 2000 Hamburg, De | |
EP0550183B1 (en) * | 1991-12-16 | 1995-09-13 | Texaco Chemical Inc. | Purification of tertiary butyl alcohol |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL288077A (en) * | 1962-01-24 | 1900-01-01 | ||
US3285977A (en) * | 1962-04-12 | 1966-11-15 | Gulf Research Development Co | Hydration of olefins in the presence of a solvent |
-
1974
- 1974-06-11 GB GB2588374A patent/GB1443106A/en not_active Expired
- 1974-06-18 CA CA202,697A patent/CA1029750A/en not_active Expired
- 1974-06-25 DE DE2430470A patent/DE2430470A1/en not_active Ceased
- 1974-07-22 FR FR7425342A patent/FR2245591B1/fr not_active Expired
- 1974-08-28 BE BE1006146A patent/BE819255A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
GB1443106A (en) | 1976-07-21 |
DE2430470A1 (en) | 1975-02-06 |
BE819255A (en) | 1974-12-16 |
CA1029750A (en) | 1978-04-18 |
FR2245591A1 (en) | 1975-04-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |