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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287113Generated: October 28, 2026

Acetic Anhydride → HCID 70567532, compound

https://huagongshe.com/reaction/2287113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantBenzene ethyl acetateHCID 21583983—
ReactantHCID 70567759HCID 70567759—
SolventDichloromethaneHCID 6344—
ProductHCID 70567532HCID 7056753281%

Reaction Steps

A mixture of (4 R,S)-4-vinylthio-(1-hydroxyethyl-2-ethoxycarbonyl)-2-oxo-azetidine (1.01 g, 4.13 mmole), acetic anhydride (1 ml, 10.6 mmole), and Et3N (0.7 ml, 5 mmole) dissolved in methylene chloride (60 ml) was allowed to stand overnight at room temperature. The reaction mixture was then washed with brine (3 times), and dried on Na2SO4. Evaporation of the solvent left a residue which, after column chromatography (SiO2, 10% ethyl acetate-benzene), yielded 950 mg (3.31 mmole, 81%) of an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04269771
Source datasetuspto-grants-1981_05
ORD IDord-dd2cd102ade94376aa285f5a23a92c7b
Source noteuspto-grants-1981_05