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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661325Generated: November 2, 2026

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

https://huagongshe.com/reaction/661325

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 numberUS08084604B2
Source datasetuspto-grants-2011_12
ORD IDord-2eb13d64df7e4f5b8ed6bcd4a8119a4d
Source noteuspto-grants-2011_12