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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046645Generated: October 27, 2026

4-Bromoaniline → HCID 178510763, compound

https://huagongshe.com/reaction/1046645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanilineHCID 7807—
Reactant(o-Chlorophenyl)acetonitrileHCID 76112—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventChloroform methanolHCID 21584188—
ProductHCID 178510763HCID 17851076348.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Bromoaniline (6.4 g, 37 mmol) was placed into a three-neck reactor, and the reactor was flushed with argon for 20 min. 60 mL anhydrous toluene was added. After cooling to 0° C., trimethylaluminum (28 mL, 2.0M solution in toluene, 56 mmol) was added slowly to keep the inner temperature below 20° C. Over 0.5 h, the addition was completed. Ice bath was removed, and the reaction mixture was warmed to room temperature and then stirred for additional 2.5 hrs. A solution of 2-chlorobenzyl cyanide (8.4 g, 55 mmol) in 35 mL anhydrous toluene was added, and the reaction mixture was heated to 80° C. After 18 hrs, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in CHCl3/MeOH (4/1, 400 mL). After stirring for 30 min, the mixture was filtered and the residue was washed with a mixture of CHCl3/MeOH (4/1). The combined filtrates were concentrated in vacuo, and the resulting solid was washed with hexane to give a light pink solid (5.78 g, 48% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569352B2
Source datasetuspto-grants-2013_10
ORD IDord-f5ec7e642343404b86726cd26ec977bc
Source noteuspto-grants-2013_10