Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:9](=[O:11])[CH3:10])[CH:5]=[CH:6][C:7]=1[F:8].[CH3:12][N:13]([CH:15](OC)OC)[CH3:14]>>[F:1][C:2]1[CH:3]=[C:4]([C:9](=[O:11])/[CH:10]=[CH:12]/[N:13]([CH3:15])[CH3:14])[CH:5]=[CH:6][C:7]=1[F:8]Participants
3
Procedure
The title compound was prepared in 84% yield from 1-(3,4-difluorophenyl)ethanone and DMF-DMA according to the procedure for the preparation of Example 12, part A. 1H NMR (400 MHz, CDCl3): δ 2.93 (3H, s), 3.16 (3H, s), 5.62 (1H, d, J=12.0 Hz), 7.13-7.20 (1H, m), 7.63-7.76 (2H, m), 7.83 (1H, d, J=12.0 Hz).
Sources & evidence
- ORD record
- ord-8e532665e6fd4c858cd1d1d1e231ffbc
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09107916B2
Linked notes
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