GB424284A - Catalytic manufacture of ethyl acetate from ethyl alcohol - Google Patents
Catalytic manufacture of ethyl acetate from ethyl alcoholInfo
- Publication number
- GB424284A GB424284A GB23133/33A GB2313333A GB424284A GB 424284 A GB424284 A GB 424284A GB 23133/33 A GB23133/33 A GB 23133/33A GB 2313333 A GB2313333 A GB 2313333A GB 424284 A GB424284 A GB 424284A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mercury
- cobalt
- cadmium
- ethyl acetate
- metals
- 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
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/39—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester
- C07C67/40—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester by oxidation of primary alcohols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
Ethyl acetate is produced by subjecting ethyl alcohol vapour to a temperature of 250--500 DEG C. and preferably 380 DEG C. in presence of a mixed chromite catalyst comprising one or more of the metals iron, nickel, and cobalt, and one or more of the metals cadmium, mercury, and tin. The reaction is preferably effected under increased pressure, e.g. 200 atmospheres. The catalysts may be prepared by mixing or by co-precipitation of the components and may or may not be reduced before use. A typical example consists of cobalt, cadmium, and mercury chromites in the molecular ratio 82,5 : 10,0 : 7,5.ALSO:Ethyl acetate is produced by subjecting ethyl alcohol vapour to a temperature of 250--500 DEG C. and preferably 380 DEG C. in presence of a mixed chromite catalyst comprising one or more of the metals iron, nickel and cobalt, and one or more of the metals cadmium, mercury and tin. The reaction is preferably effected under increased pressure, e.g. 200 atmospheres. The catalysts may be prepared by mixing or by co-precipitation of the components and may or may not be reduced before use. A typical example consists of cobalt, cadmium, and mercury chromites in the molecular ratio 82,5 : 10,0 : 7,5.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US424284XA | 1932-08-18 | 1932-08-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB424284A true GB424284A (en) | 1935-02-18 |
Family
ID=21921881
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23133/33A Expired GB424284A (en) | 1932-08-18 | 1933-08-18 | Catalytic manufacture of ethyl acetate from ethyl alcohol |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB424284A (en) |
-
1933
- 1933-08-18 GB GB23133/33A patent/GB424284A/en not_active Expired
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB558294A (en) | Catalysts and the preparation thereof | |
GB424284A (en) | Catalytic manufacture of ethyl acetate from ethyl alcohol | |
ES306124A1 (en) | Procedure of oxidation of a saturated aliciclic hydrocarbon. (Machine-translation by Google Translate, not legally binding) | |
ES432479A1 (en) | Preparation of malonic acid dialkylesters | |
GB938647A (en) | Oxide catalysts | |
IL43433A (en) | Process for preparing cycloalkanones and cycloalkanols | |
GB587181A (en) | Improvement in catalytic hydrogenation of acetophenone to phenyl methyl carbinol | |
ES289307A1 (en) | Procedure for preparing acetic acid (Machine-translation by Google Translate, not legally binding) | |
GB583344A (en) | Process for the production of lactones | |
GB1212339A (en) | Preparation of cyclododecanol | |
GB1003578A (en) | Process for the manufacture of hydroxymethylcyclododecane | |
GB1546164A (en) | Process for preparing n',n'-disubstituted acid hydrazides | |
GB1227245A (en) | ||
ES301888A3 (en) | A process of hydrocoating lubricating oils. (Machine-translation by Google Translate, not legally binding) | |
GB364134A (en) | Process for the production of higher alcohols, particularly butyl alcohol, from ethyl alcohol | |
GB400189A (en) | Improvements in or relating to the production of organic acids or esters thereof | |
GB979413A (en) | Process for activating noble metal catalyst | |
JPS52136111A (en) | Preparation of acetaldehyde | |
GB998824A (en) | Method of obtaining cyclohexanone from cyclohexanol | |
GB199027A (en) | Process for the preparation of lithium nitride in a pulverised state | |
GB434105A (en) | Improvements in or relating to the manufacture of ketones | |
GB402925A (en) | Improvements in the manufacture and production of hydro rubber | |
GB1003579A (en) | Process for the preparation of monohydroxymethyl cyclooctane | |
GB516586A (en) | Improvements in or relating to the manufacture of basic nitrogenous compounds | |
ES301769A3 (en) | A hydrocoating procedure for lubricating oils. (Machine-translation by Google Translate, not legally binding) |