돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49492생성일: 2026년 10월 24일

Water → 5-(Benzyloxy)-2,3-dihydro-1H-indole

https://huagongshe.com/ko/reaction/49492

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물5-BenzyloxyindoleHCID 14624—
반응물Potassium HydroxideHCID 14797—
반응물Sodium cyanoborohydrideHCID 5003444—
용매Acetic AcidHCID 176—
생성물5-(Benzyloxy)-2,3-dihydro-1H-indoleHCID 1679488189.2%

반응 단계

In analogy to the method described by Gordon W. Gribble, Joseph H. Hoffmann Synthesis 1977, 859-860, the following reaction was performed. To a precooled solution of 22.3 g (0.1 mol) 5-benzyloxyindole in 270 ml acetic acid, 19 g (0.3 mol) NaCNBH3 were added. The solution was stirred at RT for 2 h, the volume was reduced to one third and poured into 300 ml water. KOH was added under cooling and the solution was extracted with ether. The combined organic phases were washed with water, dried over Na2SO4 and evaporated to yield 20.1 g (89%) 5-Benzyloxy-2,3-dihydro-1H-indole as colorless oil, MS: 225 (M).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706751B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-bd86c4538ce548e0b9203acfa8be0660
출처 메모uspto-grants-2004_03