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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410234Generated: November 4, 2026

Acetonitrile → HCID 71293687, compound

https://huagongshe.com/reaction/2410234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-FluoroanilineHCID 9584—
ReactantBenzene, 2-isocyanato-1-methoxy-4-(trifluoromethyl)-HCID 11983909—
ProductHCID 71293687HCID 71293687—

Reaction Conditions

Temperature82 °C

Reaction Steps

2-Methoxy-5-trifluoromethylphenyl isocyanate (1057.8 g) is dissolved in acetonitrile (4240 ml), then 2-fluoroaniline (540.8 g) is added thereto and the mixture is rinsed in with acetonitrile (50 ml). The resulting clear solution is stirred under reflux (ca. 82° C.) for 4 h, then seeded at ca. 78° C. and stirred for ca. 15 min. The suspension is cooled to 0° C., and the product is filtered off with suction and washed with acetonitrile (950 ml, cooled to 0-5° C.). The product is dried overnight at 45° C. in a vacuum drying oven using entraining nitrogen. A total of 1380.8 g of N-(2-fluorophenyl)-N-[2-methoxy-5-(trifluoromethyl)phenyl]urea are obtained as a solid, corresponding to 86.4% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816075B2
Source datasetuspto-grants-2014_08
ORD IDord-f6c4e559c0414f11a66cab9eb9efbb6f
Source noteuspto-grants-2014_08