Thionyl Chloride → HCID 90315066, compound
Reaction equation
[F:1][C:2]1[CH:10]=[C:9]([C:11]([F:17])([F:16])[C:12]([F:15])([F:14])[F:13])[CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:20])=O>>[F:1][C:2]1[CH:10]=[C:9]([C:11]([F:17])([F:16])[C:12]([F:15])([F:14])[F:13])[CH:8]=[CH:7][C:3]=1[C:4]([Cl:20])=[O:5]Participants
3
Conditions
- Temperature
- 60 °C
Procedure
To 2-fluoro-4-(1,1,2,2,2-pentafluoroethyl)benzoic acid (1 g, 3.87 mmol) was added thionyl chloride (3.67 mL, 50.36 mmol) and the reaction was stirred at 60° C. for 22 hours. Excess thionyl chloride was removed in vacuo to yield 2-fluoro-4-(1,1,2,2,2-pentafluoroethyl)benzoyl chloride (1 g, 93%) as a viscous yellow liquid.
Workup
- customExcess thionyl chloride was removed in vacuo
Sources & evidence
- ORD record
- ord-474a27e6b3d744aea3c360023f7d21a8
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09421196B2
Reaction notes
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