GB1443106A - Process for producing tertiary butyl alcohol - Google Patents

Process for producing tertiary butyl alcohol

Info

Publication number
GB1443106A
GB1443106A GB2588374A GB2588374A GB1443106A GB 1443106 A GB1443106 A GB 1443106A GB 2588374 A GB2588374 A GB 2588374A GB 2588374 A GB2588374 A GB 2588374A GB 1443106 A GB1443106 A GB 1443106A
Authority
GB
United Kingdom
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
Application number
GB2588374A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from JP8371973A external-priority patent/JPS5622855B2/ja
Priority claimed from JP2649174A external-priority patent/JPS5314044B2/ja
Application filed by Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Publication of GB1443106A publication Critical patent/GB1443106A/en
Expired legal-status Critical Current

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.
GB2588374A 1973-07-25 1974-06-11 Process for producing tertiary butyl alcohol Expired GB1443106A (en)

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 (1)

Publication Number Publication Date
GB1443106A true GB1443106A (en) 1976-07-21

Family

ID=27159525

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2588374A Expired GB1443106A (en) 1973-07-25 1974-06-11 Process for producing tertiary butyl alcohol

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)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4284831A (en) 1979-06-26 1981-08-18 Toa Nenryo Kogyo Kabushiki Kaisha Process for the production of tertiary alcohols
US4327231A (en) 1979-04-27 1982-04-27 Toa Nenryo Kogyo Kabushiki Kaisha Process for the production of tertiary alcohols
GB2145415A (en) * 1983-08-23 1985-03-27 Humpheys & Glasgow Limited Isopropanol and tert-butanol mixtures from liquid petroleum gas
EP0550183A1 (en) * 1991-12-16 1993-07-07 Texaco Chemical Inc. Purification of tertiary butyl alcohol

Families Citing this family (6)

* Cited by examiner, † Cited by third party
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
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
DE3628008C1 (en) * 1986-08-19 1987-11-05 Deutsche Texaco Ag, 2000 Hamburg, De

Family Cites Families (2)

* Cited by examiner, † Cited by third party
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

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4327231A (en) 1979-04-27 1982-04-27 Toa Nenryo Kogyo Kabushiki Kaisha Process for the production of tertiary alcohols
US4284831A (en) 1979-06-26 1981-08-18 Toa Nenryo Kogyo Kabushiki Kaisha Process for the production of tertiary alcohols
GB2145415A (en) * 1983-08-23 1985-03-27 Humpheys & Glasgow Limited Isopropanol and tert-butanol mixtures from liquid petroleum gas
EP0550183A1 (en) * 1991-12-16 1993-07-07 Texaco Chemical Inc. Purification of tertiary butyl alcohol

Also Published As

Publication number Publication date
FR2245591B1 (en) 1978-11-24
DE2430470A1 (en) 1975-02-06
FR2245591A1 (en) 1975-04-25
BE819255A (en) 1974-12-16
CA1029750A (en) 1978-04-18

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19930611