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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1725235생성일: 2026년 10월 27일

Acetic Acid → N-heptyl-N-[(1-methylindol-2-yl)methyl]amine

https://huagongshe.com/reaction/1725235

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1-HeptanamineHCID 8127—
반응물1-Methylindole-2-carboxaldehydeHCID 267164—
반응물Sodium cyanoborohydrideHCID 5003444—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물N-heptyl-N-[(1-methylindol-2-yl)methyl]amineHCID 6885583461%

반응 단계

To a solution of 1-methylindole-2-carbaldehyde (1.59 g, 10.0 mmol) and heptylamine (1.49 mL, 10.0 mmol) in ethanol (50 mL) were added acetic acid (2.3 mL, 40 mmol) and sodium cyanoborohydride (0.75 g, 12.0 mmol) and the reaction mixture was stirred at room temperature overnight. Water (5 mL) was added and the mixture was concentrated in vacuo. The residue was taken up in ethyl acetate (75 mL) and aqueous 1 M KOH (75 mL) and the phases were separated. The aqueous layer was extracted with ethyl acetate (2×75 mL) and the combined organic phase was washed with brine (75 mL), dried over Na2SO4, and concentrated in vacuo. Purification on a column of silica gel (130 g) with ethyl acetate (17-33% gradient) in heptane as the eluent yielded 1.57 g (61%) of a yellow oil, which solidified upon standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07488844B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-184d1136bece4a75ba16d8502b7d67e2
출처 메모uspto-grants-2009_02