GB689430A - Improvements in or relating to the preparation of 2:4:5-trichlorbenzylchloride - Google Patents
Improvements in or relating to the preparation of 2:4:5-trichlorbenzylchlorideInfo
- Publication number
- GB689430A GB689430A GB8677/51A GB867751A GB689430A GB 689430 A GB689430 A GB 689430A GB 8677/51 A GB8677/51 A GB 8677/51A GB 867751 A GB867751 A GB 867751A GB 689430 A GB689430 A GB 689430A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloromethyl
- sulphuric acid
- chloromethyl ether
- acid
- excess
- 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
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/32—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by introduction of halogenated alkyl groups into ring compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
2,4,5 - Trichlorobenzylchloride is prepared by reacting 1,2,4-trichlorobenzene in a molecular excess of fuming sulphuric acid with chloromethyl ether at a temperature not substantially exceeding the boiling-point of chloromethyl ether (c.a. 59 DEG C.), e.g. within the range of from -5 DEG to 20 DEG C., or from -20 DEG to 40 DEG C. The acid may be used in a 2 to 10 fold excess over the molar proportion, but it is preferred to use an excess of from 5 to 7 mols. over the molar proportion. One example is given. The Specification also refers to the introduction of the chloromethyl group into aromatic compounds by means of chloromethyl ether and stannous chloride, or by means of formaldehyde and concentrated hydrochloric acid. Aromatic hydrocarbons containing negative substituents may be reacted with sulphuric acid, sodium chloride and paraformaldehyde or trioxymethylene to introduce chloromethyl groups. A chloromethyl group is introduced into 4-nitrotoluene with bis-chloromethyl ether and fuming sulphuric acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE689430X | 1950-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB689430A true GB689430A (en) | 1953-03-25 |
Family
ID=6598702
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8677/51A Expired GB689430A (en) | 1950-04-20 | 1951-04-13 | Improvements in or relating to the preparation of 2:4:5-trichlorbenzylchloride |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB689430A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0369728A1 (en) * | 1988-11-14 | 1990-05-23 | Ethyl Corporation | Haloalkylation of aromatic compounds |
-
1951
- 1951-04-13 GB GB8677/51A patent/GB689430A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0369728A1 (en) * | 1988-11-14 | 1990-05-23 | Ethyl Corporation | Haloalkylation of aromatic compounds |
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