関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bis(2-Methoxyethyl)amine | HCID 2383 | — |
| 反応物 | 8-Methoxy-3,4-dihydronaphthalen-1(2H)-one | HCID 11275335 | — |
| 触媒 | p-Toluenesulfonic acid | HCID 6101 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 1,2,3,4-Tetrahydro-8-methoxy-N,N-bis(2-methoxyethyl)-2-naphthalenamine | HCID 18331804 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05545755 |
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| 出典データセット | uspto-grants-1996_08 |
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| ORD ID | ord-bd3701025fd141bbb1cf73490c632a8e |
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| 出典メモ | uspto-grants-1996_08 |
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