Thionyl Chloride → 2-Chloro-4-trifluoromethyl-5-thiazolecarbonyl chloride
Reaction equation
[Cl:1][C:2]1[S:3][C:4]([C:11]([O:13]CC)=O)=[C:5]([C:7]([F:10])([F:9])[F:8])[N:6]=1.S(Cl)([Cl:18])=O>>[Cl:1][C:2]1[S:3][C:4]([C:11]([Cl:18])=[O:13])=[C:5]([C:7]([F:10])([F:9])[F:8])[N:6]=1Participants
3
Procedure
A mixture of 36.0 g (0.1554 mole) of the acid of Example 17 and 171 g (1.437 mole) of thionyl chloride were held at reflux for 6 hours. Excess thionyl chloride was removed under reduced pressure and the residue (38.1 g, 98%) was reacted as described in Examples 19-31.
Workup
- temperatureat reflux for 6 hours
- customExcess thionyl chloride was removed under reduced pressure
- customthe residue (38.1 g, 98%) was reacted
Sources & evidence
- ORD record
- ord-0cb12a5c7f1a4980879f95119b66b71c
- Source dataset
- uspto-grants-1984_03
- Patent number
- US04437875
Reaction notes
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