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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231521Generated: October 29, 2026

Phenylacetyl chloride → HCID 54479352, compound

https://huagongshe.com/reaction/2231521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
ReactantHCID 54259413HCID 54259413—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54479352HCID 5447935290.6%

Reaction Steps

To a solution of 0.387 g of (3S,4S)-4-acetoxy-3-amino-1-t-butyldimethylsilyl-2-oxoazetidine in 20 ml of THF is added 0.24 g of triethylamine under ice-cooling, and then, a solution of 0.32 g of phenylacetyl chloride in THF is added dropwise. The mixture is stirred under ice-cooling for one hour, the insolubles are filtered off, and the filtrate is concentrated under reduced pressure. Purifying the residue on a silica gel column (ethyl acetate:n-hexane-1:2) yields 0.511 g of (3S,4S)-4-acetoxy-1-t-butyldimethylsilyl-3-phenylacetamido-2-oxoazetidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04782147
Source datasetuspto-grants-1988_11
ORD IDord-591e5205ecc948a6965bc06bc0c4a875
Source noteuspto-grants-1988_11