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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53878Generated: October 29, 2026

7-Benzyl-1-tert-butoxycarbonylaminomethyl-2-oxa-7-azabicyclo[3.3.0]octane → 1-Tert-butoxycarbonylaminomethyl-2-oxa-7-aza-bicyclo[3.3.0]octane

https://huagongshe.com/reaction/53878

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyl-1-tert-butoxycarbonylaminomethyl-2-oxa-7-azabicyclo[3.3.0]octaneHCID 21704751—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Tert-butoxycarbonylaminomethyl-2-oxa-7-aza-bicyclo[3.3.0]octaneHCID 21704749—

Reaction Steps

12.2 g (34.5 mmol) of 7-benzyl-1-tert-butoxycarbonylaminomethyl-2-oxa-7-aza-bicyclo[3.3.0]octane are hydrogenated in 200 ml of ethanol on 7 g of palladium-active charcoal (10% Pd) at 100° C. and 100 bar. The catalyst is filtered off with suction and the filtrate is concentrated and distilled. Yield: 5.7 g (68% of theory) Boiling point: 120°-130° C./0.01 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05621105
Source datasetuspto-grants-1997_04
ORD IDord-c143780869ab4d41ab651f0a337b60ed
Source noteuspto-grants-1997_04