HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015557Generated: October 27, 2026
5-Methoxyadamantan-2-one → 5-Methoxy-2-methyladamantan-2-ol
https://huagongshe.com/reaction/1015557
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Methoxyadamantan-2-one | HCID 528352 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Methoxy-2-methyladamantan-2-ol | HCID 12038054 | — |
Reaction Steps
Freshly prepared methyl magnesium iodide in ether (1M, 32 mL), was added through a canula to 5-methoxyadamantan-2-one (3.0 g, 16 mmol) in THF (32 mL) at 0° C. After stirring the mixture at 0° C. for 0.5 h, the reaction mixture was quenched by adding saturated aq. NH4Cl solution. The organic layer was separated and the aqueous layer was extracted with diethyl ether. The combined organic layer was washed with water and brine, dried over anhydrous Na2SO4, and the solvent was evaporated under reduced pressure to obtain 5-methoxy-2-methyladamantan-2-ol as 1:1 anomeric mixture (3.0 g yield, 96%). m/z (M+23), 219; 1H NMR (CDCl3) 300 MHz δ 3.24 (s, 1½H), 3.23 ((s, 1½H), 2.68-2.62 (m, 1H), 2.40-1.55 (m, 10H), 1.53-1.35 (m, 2H), 1.38 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985759B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-08dbba712f724b0e95edb0041678257b |
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| Source note | uspto-grants-2011_07 |
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