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HRID 870123作成日:2026年10月25日

Sodium borohydride → 1-(3-Bromophenyl)-2-((2,4-dichlorobenzyl)(methyl)amino)ethanol

https://huagongshe.com/reaction/870123

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物1-(3-Bromophenyl)-2-((2,4-dichlorobenzyl)(methyl)amino)ethanoneHCID 67455587—
溶媒MethanolHCID 887—
生成物1-(3-Bromophenyl)-2-((2,4-dichlorobenzyl)(methyl)amino)ethanolHCID 67460028—

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08969377B2
出典データセットuspto-grants-2015_03
ORD IDord-64afcaf4ca2642d3bdac72ff61df67c9
出典メモuspto-grants-2015_03