GB883812A - Improvements in preparation of polyhydric alcohols - Google Patents
Improvements in preparation of polyhydric alcoholsInfo
- Publication number
- GB883812A GB883812A GB16098/60A GB1609860A GB883812A GB 883812 A GB883812 A GB 883812A GB 16098/60 A GB16098/60 A GB 16098/60A GB 1609860 A GB1609860 A GB 1609860A GB 883812 A GB883812 A GB 883812A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mannitol
- sorbitol
- carbon atoms
- polyhydric alcohols
- solution
- 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
- C07C29/56—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by isomerisation
-
- 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
- C07C29/132—Preparation 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
- C07C29/136—Preparation 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
- C07C29/14—Preparation 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 a —CHO group
- C07C29/141—Preparation 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 a —CHO group with hydrogen or hydrogen-containing gases
-
- 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
- C07C29/60—Preparation 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
-
- 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
- C07C31/18—Polyhydroxylic acyclic alcohols
- C07C31/26—Hexahydroxylic alcohols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Acyclic polyhydric alcohols containing 4-6 carbon atoms and one hydroxyl directly attached to each carbon atom are isomerised to similar alcohols by heating a solution of the starting alcohol in the presence of a hydrogenation catalyst at 160 DEG C.-200 DEG C. under a hydrogen pressure of 500-3,000 lbs./sq. in., for at least half an hour while maintaining the pH of the solution at 7-11, discontinuing the heating before any substantial absorption of hydrogen takes place, cooling the reaction mixture and separating the resulting solution of isomerised polyhydric alcohols from the hydrogenation catalyst. The starting alcohols may be dissolved in water, an alcohol of 1-4 carbon atoms or a glycol of 2-4 carbon atoms. Suitable hydrogenation catalysts are, for example, nickel or cobalt deposited on an inert carrier, or copper chromite. Examples are given of the isomerisation of (a) sorbitol to mannitol and iditol (b) mannitol to sorbitol and iditol; (c) dulcitol to sorbitol, mannitol, tallitol and allitol, and (d) erythritol to threitol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US883812XA | 1959-05-13 | 1959-05-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB883812A true GB883812A (en) | 1961-12-06 |
Family
ID=22211045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16098/60A Expired GB883812A (en) | 1959-05-13 | 1960-05-06 | Improvements in preparation of polyhydric alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB883812A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4292451A (en) | 1978-03-30 | 1981-09-29 | Ici Americas Inc. | High mannitol process (alkaline hydrogenation in presence of alkali metal carbonate) |
-
1960
- 1960-05-06 GB GB16098/60A patent/GB883812A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4292451A (en) | 1978-03-30 | 1981-09-29 | Ici Americas Inc. | High mannitol process (alkaline hydrogenation in presence of alkali metal carbonate) |
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