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HRID 48209作成日:2026年10月24日

Acetic Acid → N-ethyl-5-bromo-8-nitrotetrahydroisoquinoline

https://huagongshe.com/ja/reaction/48209

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5-Bromo-8-nitroisoquinolineHCID 816983—
反応物Sodium borohydrideHCID 4311764—
溶媒TetrahydrofuranHCID 8028—
生成物N-ethyl-5-bromo-8-nitrotetrahydroisoquinolineHCID 6989502670%

反応手順

A solution of 5-bromo-8-nitroisoquinoline (1 g, 3.95 mmol) in 20 mL THF was cooled to 0° C. and treated sequentially with sodium borohydride (0.75 g, 19.83 mmol) followed by the slow addition of acetic acid (20 mL). The reaction mixture was allowed to warm to room temperature, and an additional 2 equiv. of sodium borohydride was added. After quenching with water and treatment with sodium hydroxide solution to make basic, the reaction mixture was extracted with ethyl acetate. The organic residue was chromatographed on silica gel (25% ethyl acetate in hexane) to give the N-ethyl-5-bromo-8-nitrotetrahydroisoquinoline (0.8 g, 70% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703391B2
出典データセットuspto-grants-2004_03
ORD IDord-14bfbef9101f44bfbc8c35dd9bfd29e6
出典メモuspto-grants-2004_03