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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707592Generated: October 31, 2026

2-(trifluoromethyl)-4H-3,1-benzoxazin-4-one → HCID 15766706, compound

https://huagongshe.com/reaction/1707592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(trifluoromethyl)-4H-3,1-benzoxazin-4-oneHCID 914899—
Reactant3-amino-1-(4-chlorophenyl)ureaHCID 2757859—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 15766706HCID 15766706—

Reaction Conditions

Temperature100 °C

Reaction Steps

4-(p-Chlorophenyl)semicarbazide (1.49 g, 8.03 mmol) is added to a solution of 2-(trifluoromethyl)-4H-3,1-benzoxazin-4-one (1.72 g, 8.00 mmol) in pyridine (27 mL) at 100° C. The reaction mixture is stirred for 15 hours at 100° C., cooled to room temperature and concentrated in vacuo to obtain a solid. The solid is diluted with dichloromethane and the mixture is washed sequentially with 10% hydrochloric acid and water and concentrated in vacuo to obtain a tan solid. The tan solid is washed with dichloromethane and filtered. The filtrate is concentrated in vacuo to obtain a brown foam. The foam is diluted with ether and the mixture is washed sequentially with 10% hydrochloric acid, water and saturated sodium hydrogen carbonate solution, dried over anhydrous MgSO4, decolorized with carbon and concentrated in vacuo to obtain a cream colored foam. Flash chromatography of the cream colored foam using silica gel and a 3:1 dichloromethane/hexanes solution gives the title product as a white solid, 0.36 g, which is identified by 1HNMR spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354755
Source datasetuspto-grants-1994_10
ORD IDord-826c53947a2c491db51452616f97def8
Source noteuspto-grants-1994_10