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HRID 1078071作成日:2026年10月26日

Bis(2-Methoxyethyl)amine → 1,2,3,4-Tetrahydro-8-methoxy-N,N-bis(2-methoxyethyl)-2-naphthalenamine

https://huagongshe.com/reaction/1078071

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(2-Methoxyethyl)amineHCID 2383—
反応物8-Methoxy-3,4-dihydronaphthalen-1(2H)-oneHCID 11275335—
触媒p-Toluenesulfonic acidHCID 6101—
溶媒TolueneHCID 1140—
生成物1,2,3,4-Tetrahydro-8-methoxy-N,N-bis(2-methoxyethyl)-2-naphthalenamineHCID 1833180480%

反応手順

A solution of 1.76 g (10 mmol) 8-methoxy tetralone, 2.66 g (20 mmol) N,N-bis(-2methoxyethyl)amine, and 25 mg p-toluenesulfonic acid in toluene was heated to reflux under a N2 atmosphere. The flask was equipped with a Dean-Stark trap to collect H2O. TLC analysis was used to monitor the reaction. After 48 hours, the solvent was removed in vacuo. The crude ene-amine was hydrogenated using 450 mg 10% pd/C in 50 mL MeOH at 50 psi H2 for 24 hours. The reaction mixture was filtered over celite and the filtrate purified by liquid chromatography on 400 g of silica gel-60 (230-400 mesh), eluting with hexane/ethyl acetate/isopropanol (10:5:1). Fractions homogeneous by TLC were combined and concentrated in vacuo to give pure title compound as a yellow oil (2.3 g, 80%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05545755
出典データセットuspto-grants-1996_08
ORD IDord-bd3701025fd141bbb1cf73490c632a8e
出典メモuspto-grants-1996_08