N-bromobutanimide → 5-(Bromomethyl)-2-fluorobenzonitrile
Reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([CH3:10])[CH:6]=[CH:7][C:8]=1[F:9])#[N:2].[Br:11]N1C(=O)CCC1=O>C1C=CC=CC=1>[C:1]([C:3]1[CH:4]=[C:5]([CH:6]=[CH:7][C:8]=1[F:9])[CH2:10][Br:11])#[N:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3-Cyano-4-fluorotoluene (1.0 g, 7.4 mmol), N-bromosuccinimide (1.3 g, 7.4 mmol) and catalytic 2,2i-azobisisobutyronitrile (AIBN) in benzene was heated to reflux for 16 hours, evaporated to dryness and flash chromatographed over silica gel eluting with 10% ethyl acetate/hexane to provide 1.0 g of 3-cyano-4-fluorobenzyl bromide.
Workup
- temperatureto reflux for 16 hours
- customevaporated to dryness and flash
- customchromatographed over silica gel eluting with 10% ethyl acetate/hexane
Sources & evidence
- ORD record
- ord-b785f343ec5a479085321f136addd39b
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06265417B1
Reaction notes
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