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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41534생성일: 2026년 10월 23일

1-(4-Methylbenzene-1-sulfonyl)-1H-indole-3-carbaldehyde → (1-tosyl-1H-indol-3-yl)methanol

https://huagongshe.com/ko/reaction/41534

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Methylbenzene-1-sulfonyl)-1H-indole-3-carbaldehydeHCID 735817—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
생성물(1-tosyl-1H-indol-3-yl)methanolHCID 83926392.2%

반응 단계

To a solution of 1-tosyl-1H-indole-3-carbaldehyde (7 g, 23.385 mmol) in MeOH (70 mL), NaBH4 (1.77 g, 46.769 mmol) was added at 0° C. and the mixture was stirred for 10 min. The reaction mixture was allowed to warm to rt and stirring was continued for 18 h. The solvent was removed under reduced pressure at 45° C. and the crude reaction mixture was quenched with saturated aqueous ammonium chloride solution. Ethyl acetate was added and the organic layer was washed with water and brine. The organic layer was dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to yield a solid (6.5 g, 92%). [1H-NMR (CDCl3, 300 MHz) δ 8.02-7.95 (m, 1H), 7.82-7.75 (m, 2H), 7.65-7.53 (m, 2H), 7.40-7.19 (m, 4H)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530648B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-13947a147af8496a8baa8ac63ebdbe9e
출처 메모uspto-grants-2013_09