Chlorine → 3,5-Dichloro-4-methylbenzoyl chloride

HRID 363480Notes

Reaction equation

HRID 363480 reaction equation
[Cl:1]Cl.[Cl:3][C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[CH3:13])[C:7]([Cl:9])=[O:8].[Cl-].[Cl-].[Cl-].[Al+3]>ClCCl>[Cl:3][C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([Cl:1])[C:12]=1[CH3:13])[C:7]([Cl:9])=[O:8]

Participants

5

Procedure

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 stopped and the lower organic layer was recovered. The solvent was removed by distillation.

Workup

  1. customA jacketed kettle was equipped with a chiller, overhead stirrer
  2. temperaturethe resulting red-brown mixture was cooled with agitation to 3°-5°
  3. customthe reaction temperature below 10°
  4. customwas held at 0°-5°
  5. customThe reaction mixture was purged with nitrogen
  6. customslowly quenched
  7. temperaturechilled hydrochloric acid solution (4.4 parts)
  8. temperaturewhile maintaining the temperature below 5°
  9. customthe lower organic layer was recovered
  10. customThe solvent was removed by distillation

Sources & evidence

ORD record
ord-f06ee4f180a84e8d9dbda840e80d8bb6
Source dataset
uspto-grants-1999_02
Patent number
US05874466

Reaction notes

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