HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740550Generated: October 31, 2026
Chlorine → 3,5-Dichloro-4-methylbenzoyl chloride
https://huagongshe.com/reaction/1740550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 3-Chloro-4-methylbenzoyl chloride | HCID 18424211 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,5-Dichloro-4-methylbenzoyl chloride | HCID 11127919 | — |
Reaction Steps
A jacketed kettle was equipped with a chiller, overhead stirrer, thermometer, and connections to a chlorine tank and a caustic scrubber. The kettle was charged with the previously prepared 3-chloro-4-methylbenzoyl chloride (1 part) and dichloromethane (6.8 parts). Aluminum trichloride (0.8 parts) was added, and the resulting red-brown mixture was cooled with agitation to 3-5° C. Chlorine (0.37 parts) was introduced at a sufficient rate to keep the reaction temperature below 10° C. The reactor was held at 0-5° C. for 6 hours. The reaction mixture was purged with nitrogen and slowly quenched by transfering into an agitated and chilled hydrochloric acid solution (4.4 parts) while maintaining the temperature below 5° C. Agitation was topped and the lower organic layer was recovered. The solvent was removed by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05969200 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-fad84af52fad429f95354a9be9f30b8f |
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| Source note | uspto-grants-1999_10 |
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