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Chloroform → alpha-(Aminomethyl)-4-methoxybenzyl alcohol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chloroform | HCID 6212 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 2-Amino-4'-methoxyacetophenone hydrochloride | HCID 12487188 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | alpha-(Aminomethyl)-4-methoxybenzyl alcohol | HCID 3016949 | 57.9% |
反応手順
2-Amino-4′-methoxyacetophenone hydrochloride (500 mg) was dissolved in methanol (10 ml), the solution was added with sodium borohydride (188 mg), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was added with sodium borohydride (188 mg), and further stirred for 30 minutes. The reaction mixture was added with 5 N aqueous sodium hydroxide (1 ml), the mixture was stirred for 10 minutes, and then added with chloroform, and the layers were separated. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered, and then the filtrate was concentrated under reduced pressure to obtain the title compound (240 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08097708B2 |
| 出典データセット | uspto-grants-2012_01 |
| ORD ID | ord-c6b127e9f82f4e08aac86305eb34754b |
| 出典メモ | uspto-grants-2012_01 |