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HRID 53151作成日:2026年10月24日

4-Methylindole → 4-Methylindoline

https://huagongshe.com/ja/reaction/53151

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylindoleHCID 85282—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒Acetic AcidHCID 176—
生成物4-MethylindolineHCID 58370392.2%

反応手順

To a solution of 4-methylindole (7.433 g, 0.0567 mol) in 100 mL of glacial acetic acid was added NaCNBH3 (7.25 g, 0.12 mol) portionwise over 1.5 h. The reaction mixture was then concentrated in vacuo water was added and the solution was basified with 10N NaOH. The resulting mixture was extracted with ethyl acetate (×3) and the organic extract was washed (brine), dried (Na2SO4) and evaporated to give an oil. Flash chromatography (SiO2 /ethyl acetate-hexane, 1:4) of this oil gave pure 4-methylindoline (6.962 g, 92%) as an oil: 1H NMR (DMSO-d6, 200 MHz) δ6.78 (t, J=7.6 Hz, 1H), 6.33 (d, J=7.4 Hz, 1H), 6.30 (d, J=7.6 Hz, 1H), 5.36 (br s, 1H), 3.38 (t, J=8.5 Hz, 2H), 2.81 (t, J=8.5 Hz, 2H), 2.11 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618816
出典データセットuspto-grants-1997_04
ORD IDord-018dd87bdd534d888b93dd1b102cb8bb
出典メモuspto-grants-1997_04