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HRID 63582作成日:2026年10月25日

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

https://huagongshe.com/reaction/63582

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Acetaldehyde ammoniaHCID 522583—
反応物Indole-7-carboxaldehydeHCID 2734629—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
生成物2-[(1H-Indol-7-ylmethyl)amino]-ethan-1-olHCID 21950050—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447088B2
出典データセットuspto-grants-2016_09
ORD IDord-6d082143eacc4623b3cf5fbe2eb69011
出典メモuspto-grants-2016_09