Thionyl Chloride → HCID 14770839, compound
Reaction equation
[ClH:1].[F:2][C:3]1[CH:11]=[C:10]([CH:12]2[CH2:17][CH2:16][N:15]([CH3:18])[CH2:14][CH2:13]2)[C:9]([F:19])=[CH:8][C:4]=1[C:5](O)=[O:6].S(Cl)([Cl:22])=O>>[ClH:22].[F:2][C:3]1[CH:11]=[C:10]([CH:12]2[CH2:17][CH2:16][N:15]([CH3:18])[CH2:14][CH2:13]2)[C:9]([F:19])=[CH:8][C:4]=1[C:5]([Cl:1])=[O:6]Participants
3
Procedure
2.91 g (10 mmoles) of 2,5-difluoro-4-(1-methyl-4-piperidinyl)benzoic acid hydrochloride was refluxed with thionyl chloride and evaporated to afford the title compound.
Workup
- customevaporated
Sources & evidence
- ORD record
- ord-3a0e54e74b9e4ce08d99f842d4901628
- Source dataset
- uspto-grants-1992_01
- Patent number
- US05081254
Reaction notes
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