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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505942Generated: November 1, 2026

Sodium borohydride → 8-[(4-Bromophenyl)methyl]-8-azabicyclo[3.2.1]octan-3-ol

https://huagongshe.com/reaction/1505942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant8-(4-Bromobenzyl)-8-aza-bicyclo[3.2.1]octan-3-oneHCID 55106469—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product8-[(4-Bromophenyl)methyl]-8-azabicyclo[3.2.1]octan-3-olHCID 5826683390%

Reaction Steps

Sodium borohydride (95 mg, 1.50 mmol) was added to a solution of 8-(4-bromobenzyl)-8-azabicyclo-[3.2.1]octan-3-one (0.22 g, 0.75 mmol) in methanol (10 mL) and the reaction mixture was stirred for 30 minutes. The reaction was diluted with water (10 mL) and extracted into DCM (3×20 mL). The combined organic layer was washed with saturated aqueous sodium bicarbonate solution (10 mL), dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford the title compound as an off-white solid (200 mg, 90%). 1H NMR (CDCl3, 300 MHz): 7.43 (dd, J=8.3, 2.0 Hz, 3H), 7.29-7.23 (m, 2H), 3.60-3.45 (m, 2H), 3.23-3.10 (m, 2H), 2.16-1.40 (m, 8H). LCMS (Method B): RT=1.90 min, M+H+=296/298.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-ee411d89b1f64c47864a89b1f17fff96
Source noteuspto-grants-2015_12