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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728542Generated: October 25, 2026

3-Quinuclidinone → 3-Quinuclidinol hydrochloride

https://huagongshe.com/reaction/728542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-QuinuclidinoneHCID 19507—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-butyl (2S)-2-amino-3-phenylpropanoateHCID 6931633—
ReactantPyridinium chlorideHCID 10176127—
SolventMethanolHCID 887—
Product3-Quinuclidinol hydrochlorideHCID 272372574%

Reaction Steps

To a solution of 0.09 g (56.25 mmol) 3-quinuclidinone and 4.15 g (18.75 mmol) Phe-O-t-Bu in 50 ml methanol was added over a 12 hour period a solution of 2.95 g (46.9 mmol) sodium cyanoborohydride in 13 ml methanol. After stirring for an additional 8 hours, 5.78 g (50.0 mmol) pyridine hydrochloride was added and after 11/2 hours stirring, sodium chloride was removed by filtration. The filtrate was concentrated to a foam which was treated with 15 ml methanol and 50 ml ethyl acetate to give a slurry of the byproduct 3-hydroxy quinuclidine hydrochloride (74% of excess) which was removed by filtration. The filtrate was concentrate to an oil and charged with 10 ml methanol to a 5×200 cm column of LH-20 and eluted with methanol. The product fraction contained 6.54 g of a mixture of diastereomers in a 55:45 ratio as established by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049548
Source datasetuspto-grants-1991_09
ORD IDord-aca0957fb3194138a78a65b2ad4b75d2
Source noteuspto-grants-1991_09