GB529070A - Improvements in preparation of 2-chlor-meta-5-xylenol - Google Patents
Improvements in preparation of 2-chlor-meta-5-xylenolInfo
- Publication number
- GB529070A GB529070A GB1504739A GB1504739A GB529070A GB 529070 A GB529070 A GB 529070A GB 1504739 A GB1504739 A GB 1504739A GB 1504739 A GB1504739 A GB 1504739A GB 529070 A GB529070 A GB 529070A
- Authority
- GB
- United Kingdom
- Prior art keywords
- xylenol
- chlorinated
- product purified
- sulphuryl chloride
- chlor
- 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
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/62—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by introduction of halogen; by substitution of halogen atoms by other halogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
529,070. Chlorinated xylenol. GLADDEN, G. W., and COCKER, W. W. May 20, 1939, No. 15047. [Class 2 (iii)] 1 : 3 - Dimethyl - 2 - chlor - 5 - hydroxybenzene is produced from crude meta-xylenol by direct chlorination without a pre-purification process. The preferred chlorinating agent is sulphuryl chloride but chlorine may also be used. The preferred starting materials are intermediates in the preparation of pure metaxylenol and tests are described to identify suitable materials. In examples (1) an intermediate xylenol fraction is chlorinated with sulphuryl chloride, and the product purified by crystallization. (2) An intermediate xylenol fraction is chlorinated by passing in a stream of chlorine at 25‹-30‹ C., and the product purified as in example (1). (3) An intermediate xylenol fraction is chlorinated with sulphuryl chloride in a closed vessel provided with an agitator and the product purified as above.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1504739A GB529070A (en) | 1939-05-20 | 1939-05-20 | Improvements in preparation of 2-chlor-meta-5-xylenol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1504739A GB529070A (en) | 1939-05-20 | 1939-05-20 | Improvements in preparation of 2-chlor-meta-5-xylenol |
Publications (1)
Publication Number | Publication Date |
---|---|
GB529070A true GB529070A (en) | 1940-11-13 |
Family
ID=10052100
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1504739A Expired GB529070A (en) | 1939-05-20 | 1939-05-20 | Improvements in preparation of 2-chlor-meta-5-xylenol |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB529070A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102775278A (en) * | 2012-07-27 | 2012-11-14 | 湖南利洁生物化工有限公司 | Crystallization and purification method of 1-hydroxyl-3,5-dimethyl-4-chlorobenzene |
WO2023284525A1 (en) * | 2021-07-13 | 2023-01-19 | 山东新和成维生素有限公司 | Method for preparing 4-chloro-3,5-dimethylphenol by means of low-temperature chlorination |
-
1939
- 1939-05-20 GB GB1504739A patent/GB529070A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102775278A (en) * | 2012-07-27 | 2012-11-14 | 湖南利洁生物化工有限公司 | Crystallization and purification method of 1-hydroxyl-3,5-dimethyl-4-chlorobenzene |
CN102775278B (en) * | 2012-07-27 | 2014-03-05 | 湖南利洁生物化工有限公司 | Crystallization and purification method of 1-hydroxyl-3,5-dimethyl-4-chlorobenzene |
WO2023284525A1 (en) * | 2021-07-13 | 2023-01-19 | 山东新和成维生素有限公司 | Method for preparing 4-chloro-3,5-dimethylphenol by means of low-temperature chlorination |
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