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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187977Generated: 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/1187977

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 numberUS08673951B2
Source datasetuspto-grants-2014_03
ORD IDord-2e19a8447b3948e6931020d5deb5da34
Source noteuspto-grants-2014_03