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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 641886생성일: 2026년 10월 25일

Acetic Anhydride → 1-Acetyl-1H-indol-3-yl acetate

https://huagongshe.com/reaction/641886

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물Indoxyl acetateHCID 11841—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TetrahydrofuranHCID 8028—
생성물1-Acetyl-1H-indol-3-yl acetateHCID 583602—

반응 단계

Into a 500 mL round bottom flask was placed a solution of 1H-indol-3-yl acetate (8 g, 45.69 mmol) in tetrahydrofuran (150 mL). To this was added acetic anhydride (46.6 g, 456.86 mmol). Addition of triethylamine (9.25 g, 91.49 mmol) was next. To the mixture was added DMAP (1.11 g, 9.10 mmol). The resulting solution was allowed to react, with stirring, for 3 hours while the temperature was maintained at reflux in a bath of oil. The reaction progress was monitored by TLC (ethyl acetate/petroleum ether=1:2). The mixture was concentrated by evaporation under vacuum using a rotary evaporator. The resulting solution was diluted with 300 mL of ethyl acetate The resulting mixture was washed 2 times with 150 mL of NaCl(aq.). The mixture was dried over Na2SO4. The residue was purified by eluting through a column with a 20:1 petroleum ether/ethyl acetate solvent system. This resulted in 6.6 g (67%) of 1-acetyl-1H-indol-3-yl acetate as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696229B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-40cfbfe380a440d6810efc46f510a9c2
출처 메모uspto-grants-2010_04