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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Methyl-8-azabicyclo[3.2.1]octan-2-one | HCID 338156 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Methyl-2-phenyl-8-aza-bicyclo[3.2.1]octan-2-ol | HCID 58565898 | 65.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153653B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-1bc6331d8ede4ee3b9ad34f9e2b52f7b |
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| Source note | uspto-grants-2012_04 |
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