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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971402Generated: October 29, 2026

Pyridine → HCID 131711532, compound

https://huagongshe.com/reaction/971402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantHCID 13019671HCID 13019671—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131711532HCID 131711532107%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 32.6 g of benzyl α-(3ξ-carbomethoxy-7-oxo-4-oxa-2,6-diazabicyclo[3.2.0]heptan-6-yl)-α-isopropylideneacetate in 750 ml of tetrahydrofuran is dropwise added a solution of 9.5 ml of pyridine and 15.1 ml of phenylacetyl chloride in 144 ml of tetrahydrofuran over a period of 15 minutes while maintaining the temperature at -20° C. and stirring under nitrogen atmosphere. The mixture is stirred for 55 minutes, poured into 700 ml of ice water, stirred for 5 minutes and extracted with ethyl acetate. The extract is washed with an aqueous solution of sodium hydrogencarbonate and water, dried on sodium sulfate, and evaporated under reduced pressure to yield 46.4 g of benzyl α-(3ξ-carbomethoxy-2-phenylacetyl-7-oxo-4-oxa-2,6-diazabicyclo[3.2.0]heptan-6-yl)-α-isopropylideneacetate as crude product in 107% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04159984
Source datasetuspto-grants-1979_07
ORD IDord-14a4ba68bf6f41cfbbbb7176b80b2c19
Source noteuspto-grants-1979_07