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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650303Generated: November 1, 2026

Ethyl Acetate → HCID 67915270, compound

https://huagongshe.com/reaction/1650303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 53958006HCID 53958006—
ReactantHCID 57132120HCID 57132120—
SolventTolueneHCID 1140—
ProductHCID 67915270HCID 6791527063%

Reaction Steps

A solution of (3S,4R)-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-4-(3-triphenylphosphoranylidene-2-oxopropyl)-2-oxoazetidine (572 mg) and (2S)-1-allyloxycarbonyl-2-formylpyrrolidine (201.5 mg) in toluene (5 ml) was heated to reflex for three hours. Evaporation of the solvent gave a residue, which was taken up into ethyl acetate. The resultant precipitate was filtered off and washed with ethyl acetate. The filtrate and the washings were combined and evaporated in vacuo. The residue was chromatographed on silica gel (50 ml) eluting with a mixture of n-hexane and ethyl acetate (2:1-1:1-1:3 V/V) to give (3S,4R)-4-[(E)-4-{(2S)-1-allyloxycarbonylpyrrolidin-2-yl}-2-oxo-3-butenyl]-3-[(1R)-1-t-butyldimethylsilyloxyethyl]-2-oxoazetidine (297.7 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923857
Source datasetuspto-grants-1990_05
ORD IDord-e2837dd63e5a44919f0b05f321023198
Source noteuspto-grants-1990_05