Reaction equation
[Cl-].[S:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7]([OH:9])=O.[CH3:10][C:11]1[C:16]([CH3:17])=[CH:15][CH:14]=[CH:13][C:12]=1[O:18][CH3:19]>>[S:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7]([C:15]1[CH:14]=[CH:13][C:12]([O:18][CH3:19])=[C:11]([CH3:10])[C:16]=1[CH3:17])=[O:9]Participants
4
Procedure
This compound was prepared in 86% yield by using step (A) of Example 1 with the chloride of 2-thiophene carboxylic acid and 2,3-dimethyl anisole.
Workup
- customThis compound was prepared in 86% yield
Sources & evidence
- ORD record
- ord-1273e75270124de9a3250c1f7c36a043
- Source dataset
- uspto-grants-1980_04
- Patent number
- US04197309
Linked notes
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