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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462878Generated: November 1, 2026

Triethylamine → 1-(1'-Carboxy-1'-chloromethyl)-4-tritylthio-2-azetidinone

https://huagongshe.com/reaction/1462878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant1-(1'-Carboxy-1'-hydroxymethyl)-4-tritylthio-2-azetidinoneHCID 12780162—
SolventDichloromethaneHCID 6344—
Product1-(1'-Carboxy-1'-chloromethyl)-4-tritylthio-2-azetidinoneHCID 13909723—

Reaction Steps

A cooled (ice bath) solution of the triethylamine salt of 1-(1'-carboxy-1'-hydroxymethyl)-4-tritylthio-2-azetidinone (1.04 g, 2.0 mmol) in methylene chloride (5 ml) was treated dropwise, under N2, with thionyl chloride (0.16 ml, 2.2 mmol) in methylene chloride (2 ml). The solution was stirred at room temperature for 20 min and concentrated. The residue was diluted with benzene and filtered over a Celite/charcoal bed. The filtrate was evaporated in vacuo to give 870 mg (quantitative) of the title compound as an amorphous solid. It was used in the next step without further purification. ir νmax : 1775 cm-1 ; 1Hmr (CDCl3) δ: 9.22 (1H, bs), 7.27 (15H, m), 5.3 and 5.2 (1H, 2d, J=2 Hz), 4.6 (1H, m) and 2.8 ppm (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461727
Source datasetuspto-grants-1984_07
ORD IDord-fd55070837b4463383a7f1bf79424039
Source noteuspto-grants-1984_07