Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893932Generated: October 30, 2026

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

https://huagongshe.com/reaction/893932

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 numberUS04282150
Source datasetuspto-grants-1981_08
ORD IDord-3f7d363a83764a9ba64699ce5d99eb9d
Source noteuspto-grants-1981_08