関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 1-(3-Bromophenyl)-2-((2,4-dichlorobenzyl)(methyl)amino)ethanone | HCID 67455587 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-(3-Bromophenyl)-2-((2,4-dichlorobenzyl)(methyl)amino)ethanol | HCID 67460028 | — |
反応手順
Into a 1 L 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 2-((2,4-dichlorobenzyl)(methyl)amino)-1-(3-bromophenyl)ethanone (77 g, 198.97 mmol, 1.00 equiv, theoretical yield) in methanol (300 mL). This was followed by the addition of NaBH4 (15 g, 394.74 mmol, 1.98 equiv) in several batches at 0° C. The resulting solution was stirred for 30 min at 0° C. in a water/ice bath. The reaction was then quenched by the addition of 100 mL of acetone. The resulting mixture was concentrated under vacuum. The resulting solution was extracted with 3×100 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:100). This resulted in 50 g (65%) of 2-((2,4-dichlorobenzyl)(methyl)amino)-1-(3-bromophenyl)ethanol as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08969377B2 |
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| 出典データセット | uspto-grants-2015_03 |
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| ORD ID | ord-64afcaf4ca2642d3bdac72ff61df67c9 |
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| 出典メモ | uspto-grants-2015_03 |
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