Thionyl Chloride → HCID 19035209, compound
Reaction equation
[F:1][C:2]1[C:10]([C:11]([F:14])([F:13])[F:12])=[C:9]([F:15])[CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:18])=O>>[F:1][C:2]1[C:10]([C:11]([F:14])([F:13])[F:12])=[C:9]([F:15])[CH:8]=[CH:7][C:3]=1[C:4]([Cl:18])=[O:5]Participants
3
Conditions
- Temperature
- 50 °C
Procedure
19.3 g (0.085 mol) of 2,4-difluoro-3-trifluoromethylbenzoic acid are added in portions at room temperature to 130 ml of thionyl chloride. After metering has ended, the mixture is heated at 50° C. until the evolution of gas has ceased. The excess thionyl chloride is then removed by distillation and the crude product is reacted further directly.
Workup
- customThe excess thionyl chloride is then removed by distillation
- customthe crude product is reacted further directly
Sources & evidence
- ORD record
- ord-2f5d5cf8c6624651ad1aacee2d8e1d7a
- Source dataset
- uspto-grants-1995_10
- Patent number
- US05457104
Reaction notes
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