Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35693Generated: October 28, 2026

Phosgene → N-(2,2,3,3-tetrafluorobenzofuran-5-yl)-3-(4-difluoromethoxyphenyl)-4-phenylpyrazoline-1-carboxamide

https://huagongshe.com/reaction/35693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant5-Benzofuranamine, 2,2,3,3-tetrafluoro-2,3-dihydro-HCID 13784987—
Reactant3-(4-Difluoromethoxyphenyl)-4-phenylpyrazolineHCID 70408145—
CatalystTriethylamineHCID 8471—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductN-(2,2,3,3-tetrafluorobenzofuran-5-yl)-3-(4-difluoromethoxyphenyl)-4-phenylpyrazoline-1-carboxamideHCID 86742033—

Reaction Steps

A solution of 0.75 g (0.0036 mole) 5-amino-2,3-dihydro-2,2,3,3-tetrafluorobenzofuran dissolved in 109 mL of toluene was added dropwise to a stirred solution of 8.0 mL 20% phosgene in toluene. After complete addition the mixture was heated at reflux for two hours. The mixture was cooled and the solvent removed by evaporation under reduced pressure leaving a residue. This residue was dissolved in 15 mL of diethyl ether and added to a stirred solution of 1.04 g (0.0036 mole) 3-(4-difluoromethoxyphenyl)-4-phenylpyrazoline and three drops of triethylamine in 100 mL of diethyl ether. After complete addition the mixture was heated at reflux for one hour, then cooled to room temperature and stirred for approximately 18 hours. The solvent was removed from the reaction mixture by evaporation under reduced pressure leaving a solid residue. Recrystallization from ethanol provided 0.99 g of N-(2,3-dihydro-2,2,3,3-tetrafluorobenzofuran-5-yl)-3-(4-difluoromethoxyphenyl)-4-phenylpyrazoline-1-carboxamide (mp 155°-159° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767779
Source datasetuspto-grants-1988_08
ORD IDord-e27e3875d6524434a03c7d293d973f05
Source noteuspto-grants-1988_08