TW200517365A - Preparation of butanediol from γ-butyrolactone in the presence of water - Google Patents

Preparation of butanediol from γ-butyrolactone in the presence of water

Info

Publication number
TW200517365A
TW200517365A TW093133037A TW93133037A TW200517365A TW 200517365 A TW200517365 A TW 200517365A TW 093133037 A TW093133037 A TW 093133037A TW 93133037 A TW93133037 A TW 93133037A TW 200517365 A TW200517365 A TW 200517365A
Authority
TW
Taiwan
Prior art keywords
weight
butyrolactone
butanediol
water
substituted
Prior art date
Application number
TW093133037A
Other languages
Chinese (zh)
Inventor
Markus Roesch
Rolf Pinkos
Henrik Junicke
Michael Hesse
Stephan Schlitter
Alexander Weck
Gunther Windecker
Original Assignee
Basf Ag
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
Application filed by Basf Ag filed Critical Basf Ag
Publication of TW200517365A publication Critical patent/TW200517365A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • C07C29/149Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
    • C07C2523/80Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36 with zinc, cadmium or mercury

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

The present invention provides a process for preparing unsubstituted or alkyl-substituted 1,4-butanediol by catalytically hydrogenating, in the gas phase, a gas stream comprising an unsubstituted or alkyl-substituted γ-butyrolactone over a catalyst which contains ≤95% by weight, preferably from 5 to 95% by weight, in particular from 10 to 80% by weight, of CuO, and ≥5% by weight, preferably from 5 to 95% by weight, in particular from 20 to 90% by weight, of an oxidic support, wherein the gas stream comprising unsubstituted or alkyl-substituted γ-butyrolactone contains from 8 to 95% by weight, preferably from 8 to 55% by weight, more preferably from 8 to 20% by weight, of water, based on γ-butyrolactone.
TW093133037A 2003-11-05 2004-10-29 Preparation of butanediol from γ-butyrolactone in the presence of water TW200517365A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2003151697 DE10351697A1 (en) 2003-11-05 2003-11-05 Process for the preparation of butanediol from γ-butyrolactone in the presence of water

Publications (1)

Publication Number Publication Date
TW200517365A true TW200517365A (en) 2005-06-01

Family

ID=34559359

Family Applications (1)

Application Number Title Priority Date Filing Date
TW093133037A TW200517365A (en) 2003-11-05 2004-10-29 Preparation of butanediol from γ-butyrolactone in the presence of water

Country Status (3)

Country Link
DE (1) DE10351697A1 (en)
TW (1) TW200517365A (en)
WO (1) WO2005044768A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100372606C (en) * 2005-09-15 2008-03-05 复旦大学 Cu-B catalyst for preparing tetrahydrofuran by hydrogenation of dimethyl maleate and its preparation process
CN100386145C (en) * 2006-06-07 2008-05-07 山东轻工业学院 Solid catalyst for synthesizing propylene glycol ether and its preparing process

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2105379A5 (en) * 1970-09-03 1972-04-28 Nissan Chemical Ind Ltd Geo2/sb catalyst for colourless polyesters
DE2231986C2 (en) * 1972-06-29 1975-01-09 Mitsubishi Petrochemical Co. Ltd., Tokio PROCESS FOR THE PREPARATION OF 1,4 BUTANEDIOL
DE2455617C3 (en) * 1974-11-23 1982-03-18 Basf Ag, 6700 Ludwigshafen Process for the production of butanediol and / or tetrahydrofuran via the intermediate stage of γ-butyrolactone
JP2595358B2 (en) * 1989-12-07 1997-04-02 東燃株式会社 Method for producing 1,4-butanediol and tetrahydrofuran
DE10225926A1 (en) * 2002-06-11 2003-12-24 Basf Ag Process for the production of butanediol

Also Published As

Publication number Publication date
WO2005044768A1 (en) 2005-05-19
DE10351697A1 (en) 2005-06-09

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