化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1078070作成日:2026年10月25日
Sodium Hydroxide → (+-)-N-(cyclopropylmethyl)-1,2,3,4-tetrahydro-8-methoxy-2-naphthalenamine hydrochloride
https://huagongshe.com/reaction/1078070
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | 8-Methoxy-3,4-dihydronaphthalen-1(2H)-one | HCID 11275335 | — |
| 反応物 | N-methylcyclopropanamine hydrochloride | HCID 18546974 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | MeOH tetrahydrofuran | HCID 21899815 | — |
| 生成物 | (+-)-N-(cyclopropylmethyl)-1,2,3,4-tetrahydro-8-methoxy-2-naphthalenamine hydrochloride | HCID 18331788 | — |
反応手順
To a solution of 2.64 g (15 mmol) 8-methoxy tetralone, 6 g (60 mmol) methylcyclopropylamine HCl and 4.92 g (60 mmol) NaOAc in 30 mL MeOH/THF (1:1) was added HOAc dropwise to adjust the pH to 4-5. The reaction mixture stirred for 15 minutes under N2, then 1.26 g (20 mmol) NaCNBH3 was added. When the reaction was complete by TLC (24 h), 1N NaOH (20 mL) and H2O (200mL) was added to quench the reaction. The solution was extracted with CH2Cl2 (2×500 mL) and the combined organic layers were washed with brine, dried (MgSO4), filtered and concentrated in vacuo. The resulting oil was purified by liquid chromatography on 400 g of silica gel 60 (230-400m), eluting with hexane/acetone (3:1). Fractions homogeneous by TLC were combined and concentrated in vacuo to give pure compound as an oil. The HCl salt was formed by using a MeOH/HCl solution. The title compound was recovered by recrystallization as a white solid using EtOAc/MeOH (1.77 g, 44%); m.p. 216°-218° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05545755 |
|---|
| 出典データセット | uspto-grants-1996_08 |
|---|
| ORD ID | ord-0befaaf73ea74a969b2dcb92bf7f6f38 |
|---|
| 出典メモ | uspto-grants-1996_08 |
|---|