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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762681Generated: November 2, 2026

Ethanol → sodium (5R,6S)-2-amino-6-[(R)-1-hydoxyethyl]carbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/1762681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
Reactantp-nitrobenzyl (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]-carbapen-2-em-3-carboxylateHCID 14329106—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Productsodium (5R,6S)-2-amino-6-[(R)-1-hydoxyethyl]carbapen-2-em-3-carboxylateHCID 23718245—

Reaction Steps

A mixture of p-nitrobenzyl (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]carbapen-2-em-3-carboxylate (75 mg, 0.2 mmol), tetrahydrofuran (14 ml), ethanol (14 ml), deionized water (11 ml) containing sodium bicarbonate (16.8 mg, 0.2 mmol), and 10% palladium on carbon (75 mg) is shaken under hydrogen (45 psi) at ambient temperature for 2 hours. The mixture is filtered through a celite pad to remove the catalyst which is washed with water. The combined filtrate and wash is extracted with three portions of diethyl ether, concentrated under vacuum to about 10 ml volume, and lyophilized to afford sodium (5R,6S)-2-amino-6-[(R)-1-hydoxyethyl]carbapen-2-em-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04833167
Source datasetuspto-grants-1989_05
ORD IDord-7f598e2c8ad54a858a895161609a19d9
Source noteuspto-grants-1989_05