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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63582생성일: 2026년 10월 24일

Acetic Acid → 2-[(1H-Indol-7-ylmethyl)amino]-ethan-1-ol

https://huagongshe.com/ko/reaction/63582

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Acetaldehyde ammoniaHCID 522583—
반응물Indole-7-carboxaldehydeHCID 2734629—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
생성물2-[(1H-Indol-7-ylmethyl)amino]-ethan-1-olHCID 21950050—

반응 단계

To a solution of 7-formyl indole (2.4 g, 16.6 mmol) in 1,2-dichloroethane (60 mL) was added aminoethanol (1.2 mL, 19.8 mmol) followed by glacial acetic acid (2.0 mL) and sodium triacetoxyborohydride (3.5 g, 16.6 mmol). The reaction mixture was allowed to stir at room temperature for 16 hours. The reaction mixture was quenched by addition of water (10 mL) and 1.0 M sodium hydroxide (10 mL). The organic layer was then separated and the aqueous layer extracted with 1,2-dichloroethane (40 mL). The combined organic extracts were washed with saturated sodium bicarbonate (2×30 mL), water (2×50 mL), dried over anhydrous sodium sulfate and evaporated to dryness. 2-[(1H-indol-7-ylmethyl)-amino]-ethanol (4.4 g) was obtained as an oil LCMS (M+H)=189.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447088B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-6d082143eacc4623b3cf5fbe2eb69011
출처 메모uspto-grants-2016_09