Methyl isobutyrate → Methyl 3-[3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl]-2,2-dimethyl-3-oxopropanoate
Reaction equation
[CH3:1][CH:2]([CH3:7])[C:3]([O:5][CH3:6])=[O:4].[CH:8]1([CH2:11][O:12][C:13]2[CH:14]=[C:15]([CH:19]=[CH:20][C:21]=2[O:22][CH:23]([F:25])[F:24])[C:16](Cl)=[O:17])[CH2:10][CH2:9]1>>[CH:8]1([CH2:11][O:12][C:13]2[CH:14]=[C:15]([C:16](=[O:17])[C:2]([CH3:7])([CH3:1])[C:3]([O:5][CH3:6])=[O:4])[CH:19]=[CH:20][C:21]=2[O:22][CH:23]([F:25])[F:24])[CH2:10][CH2:9]1Participants
3
Procedure
Prepared analogously as described for example D1 using methyl 2-methylproponate and 3-cyclopropylmethoxy-4-difluoromethoxybenzoyl chloride as starting compounds.
Workup
- customPrepared analogously
Sources & evidence
- ORD record
- ord-2dad4a6073644e4c9188dd2f092f5cb2
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08865745B2
Reaction notes
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