Ethanol, 1-ethoxy-2,2,2-trifluoro- → 4-chloro-N-(2,2,2-trifluoro-1-hydroxyethyl)benzamide
Reaction equation
C(O[CH:4]([OH:9])[C:5]([F:8])([F:7])[F:6])C.[Cl:10][C:11]1[CH:19]=[CH:18][C:14]([C:15]([NH2:17])=[O:16])=[CH:13][CH:12]=1>>[Cl:10][C:11]1[CH:19]=[CH:18][C:14]([C:15]([NH:17][CH:4]([OH:9])[C:5]([F:6])([F:7])[F:8])=[O:16])=[CH:13][CH:12]=1Participants
3
Procedure
Trifluoroacetaldehyde ethyl hemiacetal and 4-chlorobenzamide were processed as in Example 1A to provide the desired product.
Sources & evidence
- ORD record
- ord-2b5584c0b7d04e8d8bb29ac3a5594f5a
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06645968B2
Reaction notes
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