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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26106Generated: October 31, 2026

Oxalyl chloride → 2-[4-(o-Methoxybenzenesulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxy-isocrotonic acid chloride

https://huagongshe.com/reaction/26106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-[4-(o-Methoxybenzenesulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxyisocrotonic acidHCID 70558040—
CatalystDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
Product2-[4-(o-Methoxybenzenesulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxy-isocrotonic acid chlorideHCID 88758230—

Reaction Steps

One drop of dimethylformamide in dioxane is added to a soltuion of 54 mg (0.1 mM) of 2-[4-(o-methoxybenzensulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methoxy-isocrotonic acid in 0.5 ml of a 10% strength solution of oxalyl chloride in dioxane, whereupon an evolution of gas occurs immediately. The mixture is stirred for 2 hours at room temperature and the solvent and the excess oxalyl chloride are evaporated off in vacuo. The residue is dried in a high vacuum and gives 2-[4-(o-methoxybenzenesulphonylthio)-3-phenoxyacetamido-2-oxoazetidin-1yl]-3-methoxy-isocrotonic acid chloride in the form of a slightly orange-coloured foam, IR spectrum (CH2Cl2): 5.60, 5.90 and 8.70 μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04147864
Source datasetuspto-grants-1979_04
ORD IDord-3ad033782a3e44aabdb080e5e324165e
Source noteuspto-grants-1979_04