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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252209Generated: November 1, 2026

HCID 131715512, compound → HCID 131715511, compound

https://huagongshe.com/reaction/1252209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131715512HCID 131715512—
SolventTrifluoroacetic acidHCID 6422—
SolventEthyl AcetateHCID 8857—
ProductHCID 131715511HCID 131715511—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-(4-p-methoxybenzyloxycarbonylbenzoylthio)-1-p-nitrobenzyloxycarbonyltriphenylphosphoranylidenemethyl-2-azetidinone (1.65 g) and anizole (0.54 g) in trifluoroacetic acid (4.1 ml) was stirred for 0.5 hour at 0° C. Evaporation of trifluoroacetic acid gave an oily residue which was dissolved in ethyl acetate. The ethyl acetate solution was extracted with aqueous potassium carbonate. The aqueous layer was washed with ether, acidified with hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over anhydrous sodium sulfate and evaporated to give 4-(4-carboxybenzoylthio)-1-p-nitrobenzyloxycarbonyltriphenylphosphoranylidenemethyl-2-azetidinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742052
Source datasetuspto-grants-1988_05
ORD IDord-e53e67a0f64d4d9f9a3cd0a29b8c80a7
Source noteuspto-grants-1988_05