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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878828Generated: October 26, 2026

Chloroacetyl isocyanate → N-chloroacetyl-N'-[4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]-2-methylbenzoyl]-N'-methyl urea

https://huagongshe.com/reaction/878828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl isocyanateHCID 78209—
Reactant4-(5-(3,5-Dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N,2-dimethylbenzamideHCID 66784343—
SolventTolueneHCID 1140—
ProductN-chloroacetyl-N'-[4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]-2-methylbenzoyl]-N'-methyl ureaHCID 8665446184.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a solution of 0.86 g of 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]-2-methyl-N-methyl benzoic acid amide in 10 mL of toluene, 0.36 g of chloroacetyl isocyanate was added, and stirred at 50° C. for 24 hours. After the completion of the reaction, the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography that was eluated with ethyl acetate-hexane (gradient of 0:1 to 3:2) to obtain 0.93 g of the aimed product as colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987464B2
Source datasetuspto-grants-2015_03
ORD IDord-e6c96ed979ac45ddbc5293ffd8641084
Source noteuspto-grants-2015_03