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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971422Generated: October 30, 2026

HCID 131711547, compound → HCID 131711551, compound

https://huagongshe.com/reaction/971422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131711547HCID 131711547—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131711551HCID 13171155195.1%

Reaction Steps

To a solution of 550 mg of benzyl α-(3ξ-acetyl-2-phenylacetyl-7-oxo-4-oxa-2,6-diazabicyclo[3.2.0]heptan-6-yl)-α-isopropylideneacetate in 8 ml of tetrahydrofuran is added 5% palladium carbon, and the mixture catalytically hydrogenated under atmospheric pressure for 2 hours. The insoluble material is removed by filtration, and the filtrate concentrated under reduced pressure. The residue (471 mg) is crystallized from a mixture of ether and petroleum ether to yield 421 mg of α-(3ξ-acetyl-2-phenylacetyl-7-oxo-4-oxa-2,6-diazabicyclo[3.2.0]heptan-6-yl)-α-isopropylideneacetic acid in 95% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04159984
Source datasetuspto-grants-1979_07
ORD IDord-e4b099e0ea8247a5a9b21ae88fb3aed4
Source noteuspto-grants-1979_07