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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14325생성일: 2026년 10월 25일

1H-Indole-6-carboxaldehyde → Indole

https://huagongshe.com/reaction/14325

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indole-6-carboxaldehydeHCID 2773435—
반응물Sodium borohydrideHCID 4311764—
반응물HCID 86594203HCID 86594203—
용매IsopropanolHCID 3776—
생성물IndoleHCID 79862.8%

반응 단계

To a stirred solution of 1H-indole-6-carbaldehyde (99 mg, 0.68 mmol) and tert-butyl (1S,2R)-3-amino-1-(3,5-difluorobenzyl)-2-hydroxypropylcarbamate acetate 3 (256 mg, 0.68 mmol) in 2-propanol (3 mL) was added sodium borohydride (30 mg, 0.82 mmol). The reaction mixture was stirred for 12 h., quenched with methanol, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:1 ethyl acetate/hexanes) provided indole (50 mg): 1H NMR (300 MHz, CDCl3) δ 8.41 (br s, 1H), 7.60 (d, J=8 Hz, 1H), 7.38 (s, 1H), 7.21 (t, J=3 Hz, 1H), 7.04 (dd, J=8, 1 Hz, 1H), 6.71-6.73 (m, 3H), 6.61-6.68 (m, 1H), 6.53 (s, 1H), 5.38 (br s, 2H), 4.66 (d, J=9 Hz, 1H), 3.89 (s, 2H), 3.49-3.54 (m, 1H), 2.91-2.98 (m, 1H), 2.62-2.73 (m, 3H), 1.35 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b5d89e8898184893be2e9ad5c582c649
출처 메모uspto-grants-2010_06