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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654520Generated: October 30, 2026

Hydrochloric Acid → 1-Azabicyclo[3.3.1]nonane-5-carboxylic acid hydrochloride

https://huagongshe.com/reaction/654520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Benzyl-5-(ethoxycarbonyl)-1-azoniabicyclo[3.3.1]nonane bromideHCID 19887596—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Azabicyclo[3.3.1]nonane-5-carboxylic acid hydrochlorideHCID 67759876—

Reaction Steps

A solution of ethyl 1-benzyl-1-azoniabicyclo[3.3.1]-non-5-ylcarboxylate bromide (D2, 7.90 g, 0.021 mole) in ethanol (150 ml) was hydrogenated over 10% Pd/C (700mg) at atmospheric pressure and 40° C. until the uptake of hydrogen ceased. The reaction mixture was filtered through a pad of kieselguhr and the filtrate concentrated in vacuo to leave a yellow solid, which was treated with 8M hydrochloric acid (130 ml) and heated under reflux until TLC indicated that hydrolysis was complete. The solution was concentrated to dryness in vacuo to give the title compound (D14) as a yellow solid (4.8 g), which was used in the next stage without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05132316
Source datasetuspto-grants-1992_07
ORD IDord-b7c35f2061314a539185bec3166e07db
Source noteuspto-grants-1992_07