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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387181Generated: October 30, 2026

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

https://huagongshe.com/reaction/387181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-fluoroanilineHCID 2782940—
ReactantBenzene, 2-isocyanato-1-methoxy-4-(trifluoromethyl)-HCID 11983909—
SolventAcetonitrileHCID 6342—
SolventDiisopropyl EtherHCID 7914—
Product1-(2-Bromo-6-fluorophenyl)-3-(2-methoxy-5-(trifluoromethyl)phenyl)ureaHCID 5785753087.4%

Reaction Conditions

Temperature81 °C

Reaction Steps

2-Methoxy-5-trifluoromethylphenyl isocyanate (1.19 kg) is fused at about 35° C. and dissolved in acetonitrile (4.2 l), then 2-bromo-6-fluoroaniline (870 g) is added and rinsed out with acetonitrile (380 ml). The resulting clear solution is stirred at 74-88° C. for 45 h, then concentrated in vacuo (200 mbar) at 50° C. to give a viscous magma (amount of distillate 4.4 l). This is diluted at room temperature with diisopropyl ether (1.5 l), filtered off with suction, washed with diisopropyl ether (1.15 l) and dried at 45° C. in the VDO using entraining nitrogen to constant mass (24 h). A total of 1.63 kg of N-(2-bromo-6-fluorophenyl)-N′-[2-methoxy-5-(trifluoromethyl)phenyl]urea is obtained as a solid, corresponding to 87.5% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372972B2
Source datasetuspto-grants-2013_02
ORD IDord-205c67d956684c8db8c57b7dd87c2709
Source noteuspto-grants-2013_02