Thionyl Chloride → 2-(3-Chlorophenyl)-2-methylpropanoyl chloride
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]([CH3:13])([CH3:12])[C:9](O)=[O:10])[CH:5]=[CH:6][CH:7]=1.S(Cl)([Cl:16])=O>>[Cl:1][C:2]1[CH:3]=[C:4]([C:8]([CH3:13])([CH3:12])[C:9]([Cl:16])=[O:10])[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
2-(3-Chlorophenyl)-2-methylpropanoic acid (5.7 g, 28.7 mmol) was stirred in thionyl chloride (100 mL) for 2 hours at reflux. The thionyl chloride was removed under vacuum to give the product (5.69 g).
Workup
- temperatureat reflux
- customThe thionyl chloride was removed under vacuum
Sources & evidence
- ORD record
- ord-e875b7ed7d81462790be6475de18cdd0
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07928139B2
Reaction notes
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