戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 232342作成日:2026年10月27日

Amiodarone → (2-n-Butyl-3-benzofuranyl)[4-[2-(diethylamino)ethoxy]-phenyl]methanol

https://huagongshe.com/reaction/232342

反応式

関与物質

役割名称HCID仕込み量
反応物AmiodaroneHCID 2157—
反応物Sodium borohydrideHCID 4311764—
触媒Palladium ChlorideHCID 24290—
溶媒MethanolHCID 887—
生成物(2-n-Butyl-3-benzofuranyl)[4-[2-(diethylamino)ethoxy]-phenyl]methanolHCID 1439162850%

反応手順

One mmole (645 mg) of the ketone, (2-n-butyl-3-benzofuranyl) [4-[2-(diethylamino)ethoxyl]-3,5-diiodophenyl] methanone is dissolved in 10 ml of methanol. Palladium dichloride (2 mmole, 354 mg) is added and the mixture is agitated to suspend the palladium dichloride. The temperature of the mixture is adjusted to 20° C. Sodium borohydride (10 mmole, 379 mg) is added and stirring is continued until reaction is complete (~1 hour). The palladium dichloride is removed by filtration and water is added to the filtrate. An ether extraction is performed and the product is removed from the ether phase by evaporation under reduced pressure. The produce is purified by chromatography (silica gel using methylene chloride) and results in >50% yield of the product, m.p. 203° C. (decomposes).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04851554
出典データセットuspto-grants-1989_07
ORD IDord-4e3d02fbec6d4384a8a9b076b189621a
出典メモuspto-grants-1989_07