GB736074A - Process for the manufacture of butyraldehyde - Google Patents
Process for the manufacture of butyraldehydeInfo
- Publication number
- GB736074A GB736074A GB24788/51A GB2478851A GB736074A GB 736074 A GB736074 A GB 736074A GB 24788/51 A GB24788/51 A GB 24788/51A GB 2478851 A GB2478851 A GB 2478851A GB 736074 A GB736074 A GB 736074A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogen
- catalyst
- hydrogenation
- added
- liquid
- 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
- C07C47/00—Compounds having —CHO groups
- C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
-
- 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
- C07C47/19—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen containing hydroxy groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Butyraldehyde is manufactured by a continuous process in which hydrogen is reacted with liquid crotonaldehyde under pressure and at a raised temperature in the presence of an aqueous phase and a hydrogenation catalyst, the liquid crotonaldehyde being introduced simultaneously with the hydrogen and the catalyst, and the catalyst being added as an aqueous suspension. Small quantities of an emulsifying agent may be added and the hydrogen is preferably used in excess. To obtain a good yield the hydrogenation should be conducted at a pH value of between 6.9 and 8.0. The required pH is obtained by the addition of both a carbonate and a hydroxide of an alkali or alkaline earth metal, e.g. of calcium, magnesium, sodium or potassium. Known hydrogenation catalysts may be used, e.g. nickel and cobalt catalysts and copper chromite. They may be supported on carriers, for example, on pumice powder or kieselguhr and may be activated, for example, by Cr2O3, Al2O3, ZnO or SiO2. Suitable emulsifying agents are soap or fatty acid condensation products.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE736074X | 1950-10-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB736074A true GB736074A (en) | 1955-08-31 |
Family
ID=6642259
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24788/51A Expired GB736074A (en) | 1950-10-23 | 1951-10-23 | Process for the manufacture of butyraldehyde |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB736074A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4361705A (en) * | 1981-06-29 | 1982-11-30 | Gulf Research & Development Company | Process for hydrogenating unsaturated compounds |
US4365095A (en) * | 1981-08-03 | 1982-12-21 | Gulf Research & Development Company | Process for hydrogenating unsaturated compounds |
US4394525A (en) * | 1981-06-29 | 1983-07-19 | Gulf Research & Development Company | Process for hydrogenating aldehydes |
-
1951
- 1951-10-23 GB GB24788/51A patent/GB736074A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4361705A (en) * | 1981-06-29 | 1982-11-30 | Gulf Research & Development Company | Process for hydrogenating unsaturated compounds |
US4394525A (en) * | 1981-06-29 | 1983-07-19 | Gulf Research & Development Company | Process for hydrogenating aldehydes |
US4365095A (en) * | 1981-08-03 | 1982-12-21 | Gulf Research & Development Company | Process for hydrogenating unsaturated compounds |
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