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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841821Generated: October 30, 2026

Sodium borohydride → HCID 23159132, compound

https://huagongshe.com/reaction/1841821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Benzyl-3-azabicyclo[3.3.1]nonan-9-oneHCID 15639123—
SolventMethanolHCID 887—
Product3-Benzyl-3-azabicyclo[3.3.1]nonan-9-oneHCID 15639123—
ProductHCID 23159132HCID 23159132191.5%

Reaction Steps

N-benzyl-3-azabicyclo[3.3.1]nonane-9-one (28) was synthesized according to a method described in J. Med. Chem. 1994, 37, 2831-2840. Sodium borohydride (1.49 g) was added into the MeOH (80 ml) solution of (28) (6.75 g) with chilling on ice. After its mixture was stirred for 1 hour with chilling on ice, its solvent was evaporated under reduced pressure. Water was added to its residue, which was then subjected to extraction with methylene chloride, followed by drying its organic layer with anhydrous magnesium sulfate. Its solvent was evaporated under reduced pressure to produce a crude compound (29) (6.52 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045364E1
Source datasetuspto-grants-2015_02
ORD IDord-b63101582ebc440cacbc3cc7b3dae4a2
Source noteuspto-grants-2015_02