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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482932Generated: October 30, 2026

Phosgene → (S)-1-[[(S)-3-[[(Phenylmethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]carbonyl]-2-azetidinecarboxylic acid, phenylmethyl ester

https://huagongshe.com/reaction/482932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantTriethylamineHCID 8471—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactantbenzyl N-[(3S)-2-oxoazetidin-3-yl]carbamateHCID 12834624—
ReactantAzetidine-2-carboxylic acid, benzyl ester hydrochlorideHCID 70081492—
SolventDichloromethaneHCID 6344—
Product(S)-1-[[(S)-3-[[(Phenylmethoxy)carbonyl]amino]-2-oxo-1-azetidinyl]carbonyl]-2-azetidinecarboxylic acid, phenylmethyl esterHCID 86740685—

Reaction Conditions

Temperature-5 °C

Reaction Steps

A slurry of (S)-3-[[(phenylmethoxy)carbonyl]amino]-2-azetidinone (0.78 g, 3.54 mmole) in dry dichloromethane was warmed briefly to 50° C. and then cooled to -5° C. Triethylamine (0.354 g, 3.54 mmole) and phosgene (5.7 ml of 12.5% phosgene/toluene) were added and the reaction was stirred at -5° C. for 2 hours. The reaction was concentrated to a residue and fresh dichloromethane was added. After the solution was cooled to -50° C., triethylamine (0.714 g, 7.08 mmole) and azetidine-2-carboxylic acid, benzyl ester hydrochloride (0.8 g, 3.54 mmole) were added. The reaction was stirred at -5° C. for 45 minutes. The reaction mixture was poured into 10% monobasic potassium phosphate and the dichloromethane layer was separated and washed with water and brine. After drying over sodium sulfate the solvent evaporated. The crude oil was flash chromatographed on silica (LPS-1) eluting with ethyl/acetate:hexane (1:1). Fractions containing pure compound were concentrated to give 0.622 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576749
Source datasetuspto-grants-1986_03
ORD IDord-3f6fd980ca1f400faa0f9cb04919036e
Source noteuspto-grants-1986_03