Benzoyl chloride, 3-bromo- → 2-(3-Bromobenzoyl)-4-chloro-6-fluorobenzonitrile
Reaction equation
Br[C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5].[Br:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][CH:21]=1)[C:16](Cl)=[O:17]>>[Br:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][CH:21]=1)[C:16]([C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5])=[O:17]Participants
3
Procedure
The title compound was synthesized as described for Example 64i in 55% yield starting from 2-bromo-4-chloro-6-fluorobenzonitrile (6.35 g, 27.08 mmol) and 3-bromobenzoyl chloride (3.58 mL, 27.08 mmol).
Sources & evidence
- ORD record
- ord-488c2ba9bca44412af6aa59767fb8c3e
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030500B2
Reaction notes
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