GB936321A - Low pressure hydrogenolysis of acetylenic diols to produce aliphatic monohydric alcohols - Google Patents

Low pressure hydrogenolysis of acetylenic diols to produce aliphatic monohydric alcohols

Info

Publication number
GB936321A
GB936321A GB4092161A GB4092161A GB936321A GB 936321 A GB936321 A GB 936321A GB 4092161 A GB4092161 A GB 4092161A GB 4092161 A GB4092161 A GB 4092161A GB 936321 A GB936321 A GB 936321A
Authority
GB
United Kingdom
Prior art keywords
monohydric alcohols
aliphatic monohydric
low pressure
diol
acetylenic diols
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
GB4092161A
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.)
Engelhard Industries Inc
Original Assignee
Engelhard Industries Inc
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 Engelhard Industries Inc filed Critical Engelhard Industries Inc
Publication of GB936321A publication Critical patent/GB936321A/en
Expired legal-status Critical Current

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
    • C07C29/60Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by elimination of -OH groups, e.g. by dehydration
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/44Palladium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46Ruthenium, rhodium, osmium or iridium
    • B01J23/464Rhodium
    • 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
    • C07C29/17Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds
    • 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
    • C07C29/17Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds
    • C07C29/172Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds with the obtention of a fully saturated alcohol
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • B01J37/03Precipitation; Co-precipitation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Saturated aliphatic monohydric alcohols are produced by reacting one mole of an acetylenic diol of formula:- <FORM:0936321/IV(a)/1> in which R1, R2, R3 and R4 are hydrogen or a C1 to C6 alkyl group, with three moles of hydrogen at a pressure of 1-5 atmospheres, a temperature of 20 DEG -100 DEG C., and in the presence of a catalyst containing rhodium or a mixture of rhodium and palladium. The catalyst is preferably supported on an inert carrier. The acetylenic diol may be used in solution in an aliphatic alcohol having up to six carbon atoms, or in an aliphatic acid having up to six carbon atoms. Diols used include butyne-2-diol-1,4 and 3,6-dimethyloctyne-4-diol-3,6 to give butanol and dimethyloctanol respectively.
GB4092161A 1960-11-17 1961-11-15 Low pressure hydrogenolysis of acetylenic diols to produce aliphatic monohydric alcohols Expired GB936321A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US6981560A 1960-11-17 1960-11-17

Publications (1)

Publication Number Publication Date
GB936321A true GB936321A (en) 1963-09-11

Family

ID=22091385

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4092161A Expired GB936321A (en) 1960-11-17 1961-11-15 Low pressure hydrogenolysis of acetylenic diols to produce aliphatic monohydric alcohols

Country Status (2)

Country Link
DE (1) DE1186037B (en)
GB (1) GB936321A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0044413A1 (en) * 1980-07-18 1982-01-27 BASF Aktiengesellschaft 3,6-Dimethyl-oct-1-in-3-ols and -oct-1-en-3-ols and derivatives thereof, their use as fragrances and process for preparing 3,6-dimethyl-octan-3-ol

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3114240C2 (en) * 1981-04-08 1984-11-08 Institut neftechimi&ccaron;eskogo sinteza imeni A.V. Top&ccaron;ieva Akademii Nauk SSSR, Moskva Process for the production of alkenols

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2607807A (en) * 1950-02-24 1952-08-19 Du Pont Preparation of alcohols from carboxylic acids

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0044413A1 (en) * 1980-07-18 1982-01-27 BASF Aktiengesellschaft 3,6-Dimethyl-oct-1-in-3-ols and -oct-1-en-3-ols and derivatives thereof, their use as fragrances and process for preparing 3,6-dimethyl-octan-3-ol

Also Published As

Publication number Publication date
DE1186037B (en) 1965-01-28

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