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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867532Generated: October 26, 2026

Diisopropylethylamine → 2-(Methylamino)-2-oxoethyl 1,1'-biphenyl-4-ylmethylcarbamate

https://huagongshe.com/reaction/1867532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant2-Hydroxy-N-methylacetamideHCID 223579—
Reactant4-PhenylbenzylamineHCID 344989—
SolventDichloromethaneHCID 6344—
Product2-(Methylamino)-2-oxoethyl 1,1'-biphenyl-4-ylmethylcarbamateHCID 10402417—

Reaction Steps

0.1 g (0.97 mmol) of N-methyl-2-hydroxyacetamide is admixed dropwise at ambient temperature with a solution of 0.196 g (0.97 mmol) of 4-nitrophenyl chloroformate in 3 ml of methylene chloride and 0.166 ml (0.97 mmol) of N,N-diisopropylethylamine. The mixture is stirred at ambient temperature for 45 minutes and then a solution of 0.195 g (1.067 mmol) of 4-phenylbenzylamine in 3 ml of methylene chloride and 0.166 ml (0.97 mmol) of N,N-diisopropylethylamine is added dropwise at ambient temperature. The mixture is stirred at ambient temperature for 1 hour. It is washed with saturated aqueous ammonium chloride solution, with aqueous 10% sodium carbonate solution and with saturated aqueous sodium chloride solution. The phases are separated and the organic phase is dried over sodium sulphate. The system is filtered, the filtrate is concentrated under reduced pressure and the residue is purified by chromatography on silica gel using ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632850B2
Source datasetuspto-grants-2009_12
ORD IDord-e81b64a83b3046e0870e14328cde0eb3
Source noteuspto-grants-2009_12