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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706528Generated: November 3, 2026

HCID 54255546, compound → HCID 54381947, compound

https://huagongshe.com/reaction/1706528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54255546HCID 54255546—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 54381947HCID 5438194771.1%

Reaction Steps

3-(2-Phenylacetamido)-1-(α-methoxycarbonyl-4-benzyloxybenzyl)-2-azetidinone (70 mg) was dissolved in absolute ethanol (10 ml), and to the solution, there was added 10% palladium on carbon (30 mg). The mixture was subjected to catalytic reduction in a stream of hydrogen gas at ordinary temperature and ordinary atmospheric pressure. After a calculated volume of the hydrogen gas was absorbed into the mixture in the course of 3 hours, the catalyst was removed by filtration to give a filtrate, which was evaporated to dryness under reduced pressure. The resultant residue was treated with diethyl ether to give 3-(2-phenylacetamido)-1-(α-methoxycarbonyl-4-hydroxybenzyl)-2-azetidinone (40 mg), mp 171.5° to 175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207234
Source datasetuspto-grants-1980_06
ORD IDord-0eaa4e8cf2314091bc7a487454fcb8fb
Source noteuspto-grants-1980_06