Acetic Anhydride → N-[4-Bromo-3-(trifluoromethyl)phenyl]acetamide
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[CH:4][C:3]=1[C:9]([F:12])([F:11])[F:10].[C:13](OC(=O)C)(=[O:15])[CH3:14]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:13](=[O:15])[CH3:14])=[CH:4][C:3]=1[C:9]([F:10])([F:11])[F:12]Participants
3
Procedure
A mixture of 4-bromo-3-(trifluoromethyl)phenylamine (7.2 g, 30 mmol, Aldrich) and acetic anhydride (29 mL) was stirred at room temperature for 16 h. The reaction mixture was evaporated in vacuo to give the title product as a white solid which was used in the next step without additional purification. MS (ESI, pos. ion) m/z: 484.0 (M+1).
Workup
- customThe reaction mixture was evaporated in vacuo
Sources & evidence
- ORD record
- ord-14d5a946ccb2446ab97caabaf252475e
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08026241B2
Reaction notes
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