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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225160Generated: October 31, 2026

Tetrahydrofuran → HCID 13344800, compound

https://huagongshe.com/reaction/225160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 54376555HCID 54376555—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
ProductHCID 13344800HCID 13344800—

Reaction Steps

A mixture of p-nitrobenzyl 6-ethylidene-3-[2-(p-nitrobenzyloxycarbonylamino)ethylthio]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (37 mg), PtO2 (40 mg), THF (4 ml) and EtOH (2 ml) is hydrogenated at 50 psi and 25° C., for 2.5 hrs. The catalyst is filtered off and washed thoroughly with 0.1 M pH 7 phosphate buffer (5 ml). The combined filtrate and washings are concentrated in vacuo to remove most of the organic solvents. The aqueous residue is chromatographed on a column of Dowex-50×4 (Na Form) ion-exchange resin; the product being eluted with deionized H2O. The appropriate fractions are combined and lyophilized to afford 6-ethyl-3-(2-aminoethyl)thio-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235922
Source datasetuspto-grants-1980_11
ORD IDord-1c899152476b4a08b44359add0fbb51b
Source noteuspto-grants-1980_11