GB438820A - Process for the manufacture of ª‰-bromethylbenzene - Google Patents
Process for the manufacture of ª‰-bromethylbenzeneInfo
- Publication number
- GB438820A GB438820A GB2751534A GB2751534A GB438820A GB 438820 A GB438820 A GB 438820A GB 2751534 A GB2751534 A GB 2751534A GB 2751534 A GB2751534 A GB 2751534A GB 438820 A GB438820 A GB 438820A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bromethylbenzene
- per cent
- ethylbenzene
- reaction
- solution
- 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
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/07—Preparation of halogenated hydrocarbons by addition of hydrogen halides
- C07C17/08—Preparation of halogenated hydrocarbons by addition of hydrogen halides to unsaturated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
b -Bromethylbenzene is manufactured by reacting hydrobromic acid above ordinary temperature with styrene in solution in a solvent which does not react with hydrobromic acid, e.g. ethylbenzene, chlorbenzene or bromobenzene. The reaction may be carried out in the presence of a catalyst of the peroxidic type, e.g. a peroxide or peracid. In examples: (1) hydrogen bromide is bubbled through ethylbenzene at 125 DEG C. to which a solution of styrene in ethylbenzene is added gradually; the product contains 63 per cent of a - and 30 per cent of b -bromethylbenzene; (2) the reaction of (1) is performed at 95 DEG C. in the presence of benzoylperoxide, the percentage of b -bromethylbenzene in the product being 92 per cent; (3) the reaction of (2) is carried out at 97--98 DEG C. in solution in chlorobenzene, the product containing 79 per cent of b -bromethylbenzene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2751534A GB438820A (en) | 1934-09-25 | 1934-09-25 | Process for the manufacture of ª‰-bromethylbenzene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2751534A GB438820A (en) | 1934-09-25 | 1934-09-25 | Process for the manufacture of ª‰-bromethylbenzene |
Publications (1)
Publication Number | Publication Date |
---|---|
GB438820A true GB438820A (en) | 1935-11-25 |
Family
ID=10260821
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2751534A Expired GB438820A (en) | 1934-09-25 | 1934-09-25 | Process for the manufacture of ª‰-bromethylbenzene |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB438820A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2423497A (en) * | 1942-11-04 | 1947-07-08 | Du Pont | Production of products having recurring arylethylene units with termini from a saturated halogenated alkane |
US2440801A (en) * | 1942-06-17 | 1948-05-04 | Du Pont | Process of reacting hydrogen chloride with olefinic compounds, and product |
-
1934
- 1934-09-25 GB GB2751534A patent/GB438820A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2440801A (en) * | 1942-06-17 | 1948-05-04 | Du Pont | Process of reacting hydrogen chloride with olefinic compounds, and product |
US2423497A (en) * | 1942-11-04 | 1947-07-08 | Du Pont | Production of products having recurring arylethylene units with termini from a saturated halogenated alkane |
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