戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 641886作成日:2026年10月26日

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

https://huagongshe.com/reaction/641886

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物Indoxyl acetateHCID 11841—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TetrahydrofuranHCID 8028—
生成物1-Acetyl-1H-indol-3-yl acetateHCID 583602—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07696229B2
出典データセットuspto-grants-2010_04
ORD IDord-40cfbfe380a440d6810efc46f510a9c2
出典メモuspto-grants-2010_04