2-Chloro-4-fluorobenzonitrile → 5-Bromo-2-(4-cyano-3-chlorophenoxy)-3-fluorobenzonitrile
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([F:11])[C:5]([OH:10])=[C:6]([CH:9]=1)[C:7]#[N:8].[Cl:12][C:13]1[CH:20]=[C:19](F)[CH:18]=[CH:17][C:14]=1[C:15]#[N:16]>>[Br:1][C:2]1[CH:3]=[C:4]([F:11])[C:5]([O:10][C:19]2[CH:18]=[CH:17][C:14]([C:15]#[N:16])=[C:13]([Cl:12])[CH:20]=2)=[C:6]([CH:9]=1)[C:7]#[N:8]Participants
3
Procedure
The title compound was prepared according to the method described for Preparation at 120° C. for 68 hours using 5-bromo-3-fluoro-2-hydroxybenzonitrile (WO 2006022374) and 2-chloro-4-fluorobenzonitrile.
Workup
- customdescribed for Preparation at 120° C. for 68 hours
Sources & evidence
- ORD record
- ord-80dae758a1da4423a27d1013731f4feb
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067922B2
Reaction notes
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