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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406274Generated: October 31, 2026

N-bromobutanimide → 2-(1-Bromo-ethyl)-4-fluoro-benzonitrile

https://huagongshe.com/reaction/1406274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Ethyl-4-fluorobenzonitrileHCID 23439276—
CatalystAzobisisobutyronitrileHCID 6547—
Solvent(Trifluoromethyl)benzeneHCID 7368—
Product2-(1-Bromo-ethyl)-4-fluoro-benzonitrileHCID 6820967893.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-ethyl-4-fluoro-benzonitrile (prepared according to WO 07039178, page 116) (1.14 g, 7.6 mmol) in trifluoromethyl-benzene (30 mL) was added N-bromosuccinimide (1.63 g, 9.1 mmol, 1.2 eq.) followed by azobisisobutyronitrile (0.025 g, 0.15 mmol, 0.02 eq.). The mixture was heated to 100° C. for 18 hr under an atmosphere of nitrogen and then cooled to room temperature. The mixture was filtered and filtrate partitioned with aqueous sodium sulphite solution (1M, 20 mL). The organic phase was washed with water (20 mL) and then evaporated under reduced pressure to give the title compound as a beige solid (1.62 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916593B2
Source datasetuspto-grants-2014_12
ORD IDord-cfb20df412604c48a216f192cf4672dc
Source noteuspto-grants-2014_12