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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489861Generated: November 1, 2026

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

https://huagongshe.com/reaction/1489861

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 8570820959.3%

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, 0.052 mol), treated with triethylamine (5.56 g, 0.055 mol) while maintaining the temperature below 10° 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 numberUS05679791
Source datasetuspto-grants-1997_10
ORD IDord-6b290b5f62204fbab659e81e64159af2
Source noteuspto-grants-1997_10