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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387180Generated: October 30, 2026

2-Bromo-6-fluoroaniline → 1-(2-Bromo-6-fluorophenyl)-3-(2-methoxy-5-(trifluoromethyl)phenyl)urea

https://huagongshe.com/reaction/387180

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-fluoroanilineHCID 2782940—
ReactantBenzene, 2-isocyanato-1-methoxy-4-(trifluoromethyl)-HCID 11983909—
SolventAcetonitrileHCID 6342—
Product1-(2-Bromo-6-fluorophenyl)-3-(2-methoxy-5-(trifluoromethyl)phenyl)ureaHCID 5785753099%

Reaction Conditions

Temperature85 °C

Reaction Steps

2-Methoxy-5-trifluoromethylphenyl isocyanate (274.3 g) is dissolved in acetonitrile (1 l), then 2-bromo-6-fluoroaniline (200 g) is added and rinsed out with acetonitrile (50 ml). The resulting clear solution is stirred under reflux (ca. 85° C.) for 38 h, then concentrated in vacuo at 40° C. to a viscous magma. This is filtered off with suction, washed with acetonitrile (260 ml, cooled to 0-5° C.) and dried overnight at 45° C. in the VDO using entraining nitrogen. A total of 424.3 g of N-(2-bromo-6-fluorophenyl)-N′-[2-methoxy-5-(trifluoromethyl)phenyl]urea are obtained as a solid, corresponding to 99.2% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372972B2
Source datasetuspto-grants-2013_02
ORD IDord-002806ad9e544b9a98cb6916ece8441b
Source noteuspto-grants-2013_02