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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758491Generated: November 1, 2026

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

https://huagongshe.com/reaction/1758491

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 numberUS04374065
Source datasetuspto-grants-1983_02
ORD IDord-83b418591ef6415ab78dd0a28d6546a0
Source noteuspto-grants-1983_02