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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463356Generated: October 30, 2026

Hydrochloric Acid → 2-(Dichloromethyl)-8-(trifluoromethyl)-4H-3,1-benzoxazin-4-one

https://huagongshe.com/reaction/463356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloroacetyl chlorideHCID 6593—
Reactant2-Amino-3-(trifluoromethyl)benzoic acidHCID 604569—
Product2-(Dichloromethyl)-8-(trifluoromethyl)-4H-3,1-benzoxazin-4-oneHCID 1338132194%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 17.44 g of 2-amino-3-trifluoromethylbenzoic acid prepared by the process of J. Med. Chem., Vol. 16 (2) (1973), p. 101-106 and 34.63 g of dichloroacetyl chloride was progressively heated with stirring and at about 50° C., a hardening of the mass with rapid gas evolution of regular hydrogen chloride occured for one hour. Towards 100° C., one observed a fluidization of the reaction mixture, an intensification of hydrogen chloride evolution and an increase in the temperature to 127° C. The heating was continued until hydrogen chloride evolution ceased to obtain a brown solution which was cooled in an ice bath with stirring. The mixture was vacuum filtered and the product was empasted with ether, then with methanol and was washed with methanol to obtain 23.82 g of 2-dichloromethyl-8-trifluoromethyl-4H-3,1-benzoxazine-4-one melting at 179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518775
Source datasetuspto-grants-1985_05
ORD IDord-0e7ba7e2b9db4c62af1bf340eb071604
Source noteuspto-grants-1985_05