GB741380A - Process for the production of aromatic dicarboxylic acids - Google Patents
Process for the production of aromatic dicarboxylic acidsInfo
- Publication number
- GB741380A GB741380A GB8786/53A GB878653A GB741380A GB 741380 A GB741380 A GB 741380A GB 8786/53 A GB8786/53 A GB 8786/53A GB 878653 A GB878653 A GB 878653A GB 741380 A GB741380 A GB 741380A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzene
- chloromethyl
- methyl
- produced
- employed
- 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
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/255—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting
- C07C51/265—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting having alkyl side chains which are oxidised to carboxyl groups
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 production of aromatic dicarboxylic acids comprises heating a halogeno-methyl-alkyl benzene in aqueous suspension in the presence of a base the concentration of which is from about 1 per cent to about 50 per cent and oxygen, or an oxygen-containing gas, preferably under elevated pressure from about 20 to about 250 atmospheres, and is characterized by oxidizing in the presence of an oxidation catalyst. Halogenomethyl - alkyl benzenes mentioned include 1 - chloro - methyl - 4 - methyl benzene, 1-chloromethyl - 2 - methyl benzene, 1 - bromomethyl - 4 - methyl benzene, 1 - bromomethyl - 2 - methyl benzene, 1 - chloromethyl-4 - ethyl benzene, 1 - chloromethyl - 4 - n-propyl benzene, 1 - chloromethyl - 4 - isopropyl - benzene, 1 - bromomethyl - 4 - isopropyl benzene and 1-chloromethyl-4-amyl benzene. Mixtures of these starting materials may be employed, e.g. 1-chloromethyl-4-methyl benzene and 1-chloromethyl-2-methyl benzene may be oxidized and the phthalic and terephthalic acids separated. Oxidation catalysts mentioned include the oxides and/or salts of heavy metals such as silver oxide, cobalt oxide, copper oxide, manganese or lead oxide or peroxide or naphthenates or stearates of cobalt or manganese or mixtures of such materials. Bases mentioned are sodium, potassium or calcium hydroxide solution. The process may be carried out continuously. Oxalic and carbonic acids are produced as byproducts and sufficient excess of base is preferably employed to yield an alkaline mixture on completion of the reaction. In examples: terephthalic acid containing some p-toluic acid is produced by treating 1-chloromethyl-4-methyl-benzene with air in the presence of caustic soda solution, lead oxide and lead peroxide at elevated temperature and pressure and acidifying the reaction product (1); in a similar process 1-chloromethyl-4-ethyl benzene, produced by reacting formaldehyde and ethyl benzene in the presence of hydrochloric acid, is employed as starting material (2); and in a similar process a mixture of 1-chloromethyl-4-and 2-methyl benzenes is employed as starting material, terephthalic acid is precipitated on acidification of the reaction mixture and filtered off and phthalic acid is extracted from the filtrate with ether whilst p-toluic acid is produced as a by-product.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE741380X | 1952-03-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB741380A true GB741380A (en) | 1955-11-30 |
Family
ID=6644699
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8786/53A Expired GB741380A (en) | 1952-03-31 | 1953-03-30 | Process for the production of aromatic dicarboxylic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB741380A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1080539B (en) * | 1956-05-07 | 1960-04-28 | Ici Ltd | Process for the preparation of terephthalic acid |
US2998448A (en) * | 1957-09-30 | 1961-08-29 | Sinclair Refining Co | Preparation of benzene carboxylic acids |
-
1953
- 1953-03-30 GB GB8786/53A patent/GB741380A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1080539B (en) * | 1956-05-07 | 1960-04-28 | Ici Ltd | Process for the preparation of terephthalic acid |
US2998448A (en) * | 1957-09-30 | 1961-08-29 | Sinclair Refining Co | Preparation of benzene carboxylic acids |
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