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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327392Generated: October 27, 2026

Sodium borohydride → 2-(1-Piperidinylmethyl)-1-azabicyclo[2.2.2]octan-3-ol

https://huagongshe.com/reaction/327392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-(1-Piperidinylmethyl)-1-azabicyclo[2.2.2]octan-3-oneHCID 19108415—
SolventEthanolHCID 702—
Product2-(1-Piperidinylmethyl)-1-azabicyclo[2.2.2]octan-3-olHCID 19108399—

Reaction Steps

A solution of 2-(1-piperidinylmethyl)-1-azabicyclo-[2.2.2]octan-3-one (8.90 g, 40 mmoles) in absolute ethanol (40 ml) was treated dropwise with a solution of sodium borohydride (1.15 g, 30.4 mmoles) in absolute ethanol (40 ml). The solution was stirred at room temperature for 18 hours, concentrated in vacuo, and diluted with water (100 ml). The aqueous solution was treated with potassium carbonate and extracted with ether, and the combined organic extracts were dried (MgSO4) and concentrated in vacuo. The residual solid was recrystallized from acetonitrile to afford 3.32 g (37%) of the trans isomer as colorless crystals, mp 130°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273972
Source datasetuspto-grants-1993_12
ORD IDord-7125ac8d6b49492da0487bf64d49929b
Source noteuspto-grants-1993_12