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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050383Generated: November 2, 2026

Lactic Acid → cis-4-Oxo-3-phenoxyacetylamino-2-p-toluenesulfonyloxymethylazetidine

https://huagongshe.com/reaction/2050383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLactic AcidHCID 612—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHexaneHCID 8058—
ReactantHCID 70579374HCID 70579374—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Productcis-4-Oxo-3-phenoxyacetylamino-2-p-toluenesulfonyloxymethylazetidineHCID 86734329—

Reaction Steps

To a solution of 4.30 g (0.022 mole) of 98% p-toluenesulfonyl chloride in 24 ml of anhydrous pyridine at 0° (ice bath) was added 2.64 g (0.011 mole) of cis-2-hydroxymethyl-4-oxo-3-phenoxyacetylaminoazetidine in one portion. The solution was stirred at 0° for 3 hours then was stored at -25° overnight. After warming to 0°, 1.0 ml of 85% lactic acid was added and stirring was continued for 1 hour. The reaction mixture was poured into ethyl acetate and extracted successively with water, dilute aqueous hydrochloric acid, aqueous sodium bicarbonate and brine and was dried (MgSO4). Filtration followed by removal of the solvent in vacuo resulted in a yellow solid. Clarification of a hot solution of this material in ethyl acetate (375 ml), followed by the addition of hexane (200 ml) and recrystallization afforded cis-4-oxo-3-phenoxyacetylamino-2-p-toluenesulfonyloxymethylazetidine; tlc: ethyl acetate, silica gel GF, Rf=0.47; mp 136° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200572
Source datasetuspto-grants-1980_04
ORD IDord-610353e665a1442190ff2f8ae998d3f0
Source noteuspto-grants-1980_04