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HRID 1015556作成日:2026年10月27日

Methyl iodide → 5-Methoxyadamantan-2-one

https://huagongshe.com/reaction/1015556

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物TetrahydrofuranHCID 8028—
反応物Sodium hydrideHCID 24758—
反応物1-Hydroxyadamantan-2-oneHCID 10964884—
生成物5-Methoxyadamantan-2-oneHCID 52835283%

反応手順

To a suspension of NaH (60% dispersed in nujol, 0.96 g, 24 mmol) in THF (40 mL) cooled to ice bath temperature was added hydroxyadamantanone (3.32 g, 20 mmol) dissolved in THF (40 mL) via a syringe over a period of 15 minutes. After stirring the reaction mixture for 30 min., iodomethane (1.38 mL, 22 mmol) was added. The reaction mixture was warmed to room temperature and stirred for 16 h until TLC revealed completion of the reaction. Excess NaH was quenched by adding saturated aq. NH4Cl solution to the ice cooled reaction mixture. The two layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layer was washed with brine, dried over anhydrous Na2SO4, and the solvent was evaporated under reduced pressure to obtain crude reaction mass which was purified by column chromatography to yield 5-methoxyadamantan-2-one (3.0 g) in 83% yield. m/z (M+1), 181; 1H NMR (CDCl3) 300 MHz δ 3.26 (s, 3H), 2.67-2.61 (m, 2H), 2.39-2.33 (m, 1H), 2.20-1.93 (m, 10H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07985759B2
出典データセットuspto-grants-2011_07
ORD IDord-9d9dfdb63cbe4460be7c3461ada9ed20
出典メモuspto-grants-2011_07