GB749186A - Process for preparing ú-di-isopropyl benzene and terephthalic acid - Google Patents
Process for preparing ú-di-isopropyl benzene and terephthalic acidInfo
- Publication number
- GB749186A GB749186A GB634453A GB634453A GB749186A GB 749186 A GB749186 A GB 749186A GB 634453 A GB634453 A GB 634453A GB 634453 A GB634453 A GB 634453A GB 749186 A GB749186 A GB 749186A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzene
- acid
- isopropyl
- boron fluoride
- alkylation
- 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
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
-
- 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
Abstract
A continuous process for the preparation of p-di-isopropylbenzene comprises alkylating benzene or cumene or a mixture thereof to form a product containing o-, m- and p-di-isopropyl benzenes, subjecting the product to a distillation to separate p-di-isopropyl benzene, a fraction containing o- and m-di-isopropyl benzenes and higher boiling fractions, de-alkylating the mixture of o- and m-isomers to yield benzene and cumene which is recycled to the alkylation stage. The p. di-isopropyl benzene may be oxidized either by 10-40 per cent nitric acid, or by catalytic air oxidation in the liquid phase, e.g. as described in Specification 737,439 to form terephthalic acid. As alkylation catalyst sulphuric acid is preferred, although aluminium chloride, boron fluoride, boron fluoride with phosphoric acid, hydrofluoric acid, aluminium silicates, phosphoric acid on kieselguhr and titanium tetrachloride may also be used. The de-alkylation is preferably carried out in the presence of a solid catalyst such as mixtures of Al2O3 and SiO2, small quantities of ZrO2 may also be present. Al2O3 containing a small amount of HF, aluminium chloride, and boron fluoride may also be used. The temperature may be between 150 DEG and 600 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB634453A GB749186A (en) | 1953-03-06 | 1953-03-06 | Process for preparing ú-di-isopropyl benzene and terephthalic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB634453A GB749186A (en) | 1953-03-06 | 1953-03-06 | Process for preparing ú-di-isopropyl benzene and terephthalic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
GB749186A true GB749186A (en) | 1956-05-23 |
Family
ID=9812775
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB634453A Expired GB749186A (en) | 1953-03-06 | 1953-03-06 | Process for preparing ú-di-isopropyl benzene and terephthalic acid |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB749186A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2848514A (en) * | 1954-07-30 | 1958-08-19 | Shell Dev | Process for producing diisopropyl benzenes |
US2881227A (en) * | 1954-10-22 | 1959-04-07 | Shell Dev | Production of dhsopropyl benzenes |
DE1079027B (en) * | 1956-07-23 | 1960-04-07 | Bataafsche Petroleum | Process for the production of terephthalic acid and / or isophthalic acid |
DE1226552B (en) * | 1956-07-23 | 1966-10-13 | Universal Oil Prod Co | Process for the preparation of a selected isomer of a polyalkylated aromatic hydrocarbon |
-
1953
- 1953-03-06 GB GB634453A patent/GB749186A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2848514A (en) * | 1954-07-30 | 1958-08-19 | Shell Dev | Process for producing diisopropyl benzenes |
US2881227A (en) * | 1954-10-22 | 1959-04-07 | Shell Dev | Production of dhsopropyl benzenes |
DE1079027B (en) * | 1956-07-23 | 1960-04-07 | Bataafsche Petroleum | Process for the production of terephthalic acid and / or isophthalic acid |
DE1226552B (en) * | 1956-07-23 | 1966-10-13 | Universal Oil Prod Co | Process for the preparation of a selected isomer of a polyalkylated aromatic hydrocarbon |
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