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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257418Generated: November 2, 2026

1-Benzyl-4-(ethoxycarbonyl)-1-azoniabicyclo[2.2.1]heptane bromide → Ethyl 1-azabicyclo[2.2.1]heptane-4-carboxylate hydrobromide

https://huagongshe.com/reaction/2257418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(ethoxycarbonyl)-1-azoniabicyclo[2.2.1]heptane bromideHCID 22922780—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 1-azabicyclo[2.2.1]heptane-4-carboxylate hydrobromideHCID 22922786—

Reaction Steps

A suspension of ethyl 1-benzyl-1-azoniabicyclo[2.2.1]hept-4-ylcarboxylate bromide (D16, 130 g, 0.38 mole) in ethanol (500 ml) was hydrogenated over 10% palladium on charcoal catalyst (8 g) at atmospheric temperature and pressure for 18 h. The catalyst was removed by filtering through celite, washing several times with hot ethanol, and the filtrate concentrated in vacuo to give the title compound (D17) as a crystalline white solid (80.1 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE035593
Source datasetuspto-grants-1997_08
ORD IDord-0de1d4a0b35b46cfaf4d0a11d046fdc0
Source noteuspto-grants-1997_08