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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847211Generated: October 30, 2026

2,3-Dihydrofuran → p-nitrobenzyl (5R,6S)-6-[(R)-1-hydroxyethyl]-2-[4-(2-hydroxyethyl)-1,2,3-triazol-1-yl]carbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/847211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DihydrofuranHCID 70934—
ReactantSodium BicarbonateHCID 516892—
Reactantp-nitrobenzyl (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]-carbapen-2-em-3-carboxylateHCID 14329106—
SolventTetrahydrofuranHCID 8028—
Productp-nitrobenzyl (5R,6S)-6-[(R)-1-hydroxyethyl]-2-[4-(2-hydroxyethyl)-1,2,3-triazol-1-yl]carbapen-2-em-3-carboxylateHCID 14329122—

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) and 2,3-dihydrofuran (0.25 ml) in anhydrous tetrahydrofuran (5 ml) containing excess sodium bicarbonate is kept at 4° C. for 1 week. The mixture is filtered and the filtrate evaporated under vacuum. The residue is purified by preparative thin layer chromatography on silica gel to afford p-nitrobenzyl (5R,6S)-6-[(R)-1-hydroxyethyl]-2-[4-(2-hydroxyethyl)-1,2,3-triazol-1-yl]carbapen-2-em-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05140030
Source datasetuspto-grants-1992_08
ORD IDord-a959b9e3656a446296cbcedbc6438e7e
Source noteuspto-grants-1992_08