戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 877074作成日:2026年10月26日

Benzylamine → 1-Benzyl-4-methyl-1,4-azaphosphinane 4-oxide

https://huagongshe.com/reaction/877074

反応式

関与物質

役割名称HCID仕込み量
反応物BenzylamineHCID 7504—
反応物TetrahydrofuranHCID 8028—
反応物Methyl phosphonic dichlorideHCID 12671—
反応物Ammonium ChlorideHCID 25517—
反応物HCID 178461836HCID 178461836—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物1-Benzyl-4-methyl-1,4-azaphosphinane 4-oxideHCID 6683324651%

反応条件

温度0 °C

反応手順

To a vigorously stirred solution of methylphosphonic dichloride (6.65 g, 50 mmol) in THF (100 mL) at −78° C. was added vinylmagnesium chloride (1.6 M in THF, 66 mL, 105 mmol) dropwisely over 30 min. After the addition is completed, the reaction mixture was warmed to 0° C. over 1 hour, and to it was added benzylamine (6.43 g, 60 mmol) and methanol (100 mL). The reaction mixture was then refluxed for 36 hours. After cooled to room temperature, the reaction mixture was poured into a separation funnel containing saturated aqueous ammonium chloride (100 mL), ethyl acetate (200 mL) and water (100 mL). The organic layer was separated, and the aqueous layer was extracted with methylene chloride (100 mL) twice. The combined organic layer and extracts were dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography, eluting with 20% methanol in dichloromethane to give the desired product as white crystalline solid (5.69 g, 51%). LCMS ESI(+) m/z: 224 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08987284B2
出典データセットuspto-grants-2015_03
ORD IDord-dc8905d3763642f3bbc4290eadcfc9d6
出典メモuspto-grants-2015_03