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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499737Generated: October 31, 2026

Dimethylformamide → 2-Bromo-6-chloro-4-(1-chloroethyl)-3-ethoxybenzonitrile

https://huagongshe.com/reaction/1499737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDichloromethaneHCID 6344—
ReactantCyanuric chlorideHCID 7954—
Reactant2-Bromo-6-chloro-3-ethoxy-4-(1-hydroxyethyl)benzonitrileHCID 86677666—
Product2-Bromo-6-chloro-4-(1-chloroethyl)-3-ethoxybenzonitrileHCID 8667766775.8%

Reaction Steps

Cyanuric chloride (0.11 g, 0.59 mmol) was dissolved in N,N-dimethylformamide (3 mL, 40 mmol). After stirring for a few minutes, a solution of 2-bromo-6-chloro-3-ethoxy-4-(1-hydroxyethyl)benzonitrile (150 mg, 0.49 mmol) in methylene chloride (3 mL, 50 mmol) was added. The resulting mixture was stirred at room temperature overnight. The reaction was partitioned between water and dichloromethane. The organic layer was washed with sat. NaHCO3 solution, water, brine, dried over MgSO4, and concentrated. The crude product was purified by flash column chromatography, eluting a gradient of 0-30% EtOAc/Hexane to give 2-bromo-6-chloro-4-(1-chloroethyl)-3-ethoxybenzonitrile (0.12 gm, 75%) as a semisolid, LCMS calculated for C11H10BrCl2NO m/z=323.9, 320.9; found: (poor ionization).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199982B2
Source datasetuspto-grants-2015_12
ORD IDord-2cfc2100b04a4906aac43b8cb25f2f0b
Source noteuspto-grants-2015_12