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HRID 1818509作成日:2026年10月25日

Methyl iodide → 3-[Methoxy-(4-triisopropylsilanyloxymethyl-phenyl)-methyl]-benzonitrile

https://huagongshe.com/reaction/1818509

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3-[Hydroxy-(4-triisopropylsilanyloxymethyl-phenyl)-methyl]-benzonitrileHCID 66699612—
溶媒Sodium BicarbonateHCID 516892—
生成物3-[Methoxy-(4-triisopropylsilanyloxymethyl-phenyl)-methyl]-benzonitrileHCID 6669956360%

反応手順

A solution of 3-[hydroxy-(4-triisopropylsilanyloxymethyl-phenyl)-methyl]-benzonitrile (0.64 g, 1.62 mmol) and tetrahydrofuran (10 mL) is stirred at 0° C. Sodium hydride, 60% in mineral oil, (80 mg, 1.95 mmol) is added and the mixture is stirred at room temperature 10 min. The mixture is cooled to 0° C. and iodomethane (0.12 mL, 1.8 mmol) is added. The resulting mixture is stirred at room temperature 18 hr. The mixture is diluted with aqueous saturated sodium hydrogen carbonate, extracted with ethyl acetate, and the organic layer concentrated. The residue is purified via silica chromatography eluting with hexanes to 9:1 hexanes:ethyl acetate to provide 400 mg, 60% the title compound, as a colorless oil. 1H NMR (CDCl3) δ 7.70 (s, 1H), 7.55-7.69 (m, 2H), 7.27-7.46 (m, 5H), 5.27 (s, 1H), 4.88 (s, 2H), 3.41 (s, 3H), 1.05-1.29 (m, 21H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07598423B2
出典データセットuspto-grants-2009_10
ORD IDord-f5f1e119638d4b64b488ee5c2ed839e8
出典メモuspto-grants-2009_10