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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53151생성일: 2026년 10월 23일

4-Methylindole → 4-Methylindoline

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

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylindoleHCID 85282—
반응물Sodium cyanoborohydrideHCID 5003444—
용매Acetic AcidHCID 176—
생성물4-MethylindolineHCID 58370392.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618816
출처 데이터셋uspto-grants-1997_04
ORD IDord-018dd87bdd534d888b93dd1b102cb8bb
출처 메모uspto-grants-1997_04