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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638122Generated: November 2, 2026

Pyridine → HCID 13232644, compound

https://huagongshe.com/reaction/638122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantHCID 13232641HCID 13232641—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 13232644HCID 13232644—

Reaction Conditions

Temperature25 °C

Reaction Steps

In 100 ml of methylene chloride were dissolved under ice-cooling 5 g of p-toluenesulfonate of (3S, 4RS)-3-amino-4-cyano-2-azetidinone and 4.2 g of pyridine. To the solution was added 3 g of phenylacetyl chloride. The mixture was stirred at room temperature (about 25° C.) for ten minutes, which was shaken with water. The organic layer was separated and dried on anhydrous magnesium sulfate, then concentrated under reduced pressure. The concentrate was purified on a silicagel column chromatography [ethyl acetate:n-hexane (2:1)] to yield 1.16 g of (3S, 4S)-4-cyano-3-phenylacetamido-2-azetidinone (A) and subsequently 0.84 g of a corresponding (3S, 4R)-derivative (B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560508
Source datasetuspto-grants-1985_12
ORD IDord-be4cd869c0f54a15acdce1d2b4361c42
Source noteuspto-grants-1985_12