GB830886A - Improvements in or relating to the preparation of carboxylic compounds - Google Patents
Improvements in or relating to the preparation of carboxylic compoundsInfo
- Publication number
- GB830886A GB830886A GB2784058A GB2784058A GB830886A GB 830886 A GB830886 A GB 830886A GB 2784058 A GB2784058 A GB 2784058A GB 2784058 A GB2784058 A GB 2784058A GB 830886 A GB830886 A GB 830886A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali metal
- propionic acid
- cresol
- phenol
- salts
- 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
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process for the preparation of propionic acid or salts thereof comprises contacting an alkali metal or alkaline earth metal salt of o-cresol with at least one of hydrogen, cycloaliphatic hydrocarbons, alkali metal hydrides and alkali metal borohydrides at elevated temperature and pressure and thereafter recovering the propionic acid or salts thereof so formed. Cycloaliphatic hydrocarbons mentioned include cyclohexane, methyl and ethyl cyclohexanes, 1,2-dimethyl-cyclohexane, cyclopentane, tetra- and decahydronaphthalenes. Phenol is produced simultaneously. Mixtures of phenols containing o-cresol, e.g. cresylic acid containing a - and b -methyl naphthalenes may be employed as starting materials. The o-cresol, optionally with other phenols, may be neutralized with, e.g., alkali metal hydroxides or alkaline earth metal oxides or hydroxides. An alkali is preferably added to the reaction mixture in excess. Alkali metal carbonates are also stated to be suitable for use in the process. The free propionic acid and phenol may be obtained by treating the reacted mixture with acidic material, e.g. sulphonic or hydrochloric acid, carbon or sulphur dioxide. The reactant melt may be anhydrous or may contain some water. The propionic acid may be recovered in the form of the sodium, potassium, ammonium, barium or calcium salt. Examples are furnished.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2784058A GB830886A (en) | 1958-08-29 | 1958-08-29 | Improvements in or relating to the preparation of carboxylic compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2784058A GB830886A (en) | 1958-08-29 | 1958-08-29 | Improvements in or relating to the preparation of carboxylic compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB830886A true GB830886A (en) | 1960-03-23 |
Family
ID=10266152
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2784058A Expired GB830886A (en) | 1958-08-29 | 1958-08-29 | Improvements in or relating to the preparation of carboxylic compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB830886A (en) |
-
1958
- 1958-08-29 GB GB2784058A patent/GB830886A/en not_active Expired
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