Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680323Generated: November 1, 2026

Thionyl Chloride → p-Nitrobenzyl 2-(4-Acetylthio-2-oxo-1-azetidinyl)-2-chloroacetate

https://huagongshe.com/reaction/1680323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactantp-Nitrobenzyl 2-(4-acetylthio-2-oxo-1-azetidinyl)-2-hydroxyacetateHCID 13132061—
SolventDichloromethaneHCID 6344—
Productp-Nitrobenzyl 2-(4-Acetylthio-2-oxo-1-azetidinyl)-2-chloroacetateHCID 1313206299%

Reaction Steps

A solution of acid 1 (19.36 g), thionyl chloride (40 ml) and dichloromethane (200 ml) was stirred at 23° for 18 h. The solvent and excess thionyl chloride were evaporated in vacuo at 23° to give acid chloride 2 as an off-white solid, 20.5 g (99% yield). ##STR123##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04272437
Source datasetuspto-grants-1981_06
ORD IDord-ffa8268d9854461896c907dc44f8e3ac
Source noteuspto-grants-1981_06