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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363166Generated: October 25, 2026

Water → N-[(4-Fluoro-3-nitrophenyl)carbamoyl]glycine, ethyl ester

https://huagongshe.com/reaction/363166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Fluoro-3-nitrophenyl isocyanateHCID 144117—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
SolventTetrahydrofuranHCID 8028—
ProductN-[(4-Fluoro-3-nitrophenyl)carbamoyl]glycine, ethyl esterHCID 8570820956.1%

Reaction Steps

A solution of 4-fluoro-3-nitrophenyl isocyanate (10 g, 0.055 mol) in anhydrous tetrahydrofuran is cooled to 0° C., treated with glycine ethyl ester hydrochloride (7.7 g, 0.055 mol), treated with triethylamine (5.56 g, 0.055 mol) while maintaining the temperature below 100° C., stirred at room temperature for 1 hour and poured into water. The aqueous mixture is extracted with ether. The combined organic extracts are washed sequentially with 1N hydrochloric acid and brine, dried over anhydrous, magnesium sulfate, and concentrated in vacuo to obtain a solid which is air-dried to give the title product as a yellow solid (8.8 g, mp 115°-120° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872253
Source datasetuspto-grants-1999_02
ORD IDord-f1fe8bc5cbd84f3ca2ce9234f76f87e5
Source noteuspto-grants-1999_02