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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690268Generated: October 26, 2026

8-Methyl-8-azabicyclo[3.2.1]octan-2-one → 8-Methyl-2-phenyl-8-aza-bicyclo[3.2.1]octan-2-ol

https://huagongshe.com/reaction/1690268

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Methyl-8-azabicyclo[3.2.1]octan-2-oneHCID 338156—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product8-Methyl-2-phenyl-8-aza-bicyclo[3.2.1]octan-2-olHCID 5856589865.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 5.4 ml (5.39 mmol) of a 1M phenyl-magnesium bromide solution under nitrogen at 0° C., was added drop-wise a solution of 500 mg 8-methyl-8-aza-bicyclo[3.2.1]octan-2-one (CAS 78477-91-5) in 5 ml tetrahydrofuran over mol-sieve. The reaction mixture was stirred at 0° C. for 5 hours. The mixture was quenched under ice bath cooling with a 20% ammonium chloride solution (5 ml). The organic layer was separated and the aqueous layer was extracted once with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated in vacuo. The crude oil was purified with flash column chromatography on silica (20 g) eluting with a gradient formed from n-heptane and ethyl acetate (0 to 100%) to provide 508 mg (65.1%) of the title compound as a light yellow oil. MS (m/e): 218.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153653B2
Source datasetuspto-grants-2012_04
ORD IDord-1bc6331d8ede4ee3b9ad34f9e2b52f7b
Source noteuspto-grants-2012_04