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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057431Generated: November 1, 2026

HCID 12552203, compound → HCID 20332218, compound

https://huagongshe.com/reaction/2057431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12552203HCID 12552203—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 20332218HCID 2033221875.7%

Reaction Steps

A catalyst of 10% palladium on charcoal (Engelhard 4505, 50 mg) suspended in 90% aqueous ethanol (10 ml) was prehydrogenated for 20 minutes at room temperature/atmospheric pressure. Benzyl 7-oxo-3-p-nitrophenylthio-1-azabicyclo [3.2.0]hept-2-ene-2-carboxylate (50 mg) partially dissolved in ethanol (10 ml) was added, and the mixture was hydrogenated at room temperature and atmospheric pressure for 1.5 hours. The catalyst was removed by filtration through "High-Flo", and the colourless filtrate was evaporated to give an oil (35 mg) identical by TLC, u.v. and I.R. to the product (22) obtained in Example 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04210661
Source datasetuspto-grants-1980_07
ORD IDord-9fd4ae94c1524a4d99b4af63061147a0
Source noteuspto-grants-1980_07