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HRID 350822作成日:2026年10月27日

Phenethylamine → 8-(N-Benzyl-N-methylamino)octan-1-ol

https://huagongshe.com/reaction/350822

反応式

関与物質

役割名称HCID仕込み量
反応物PhenethylamineHCID 1001—
反応物Sodium IodideHCID 5238—
反応物AcetonitrileHCID 6342—
反応物Sodium CarbonateHCID 10340—
反応物1-Octanol, 8-chloro-HCID 90012—
溶媒tert-Butyl methyl etherHCID 15413—
生成物8-(N-Benzyl-N-methylamino)octan-1-olHCID 1666215396%

反応条件

温度80 °C

反応手順

From 8-Chlorooctan-1-ol: A 2-L flask was charged with benzylmethylamine (270 g, 2.23 mol), sodium carbonate (157 g, 1.48 mol), sodium iodide (11.1 g, 0.074 mol), 8-chlorooctanol (122 g, 0.74 mol) and acetonitrile (1000 mL) and the resulting suspension was stirred at 80° C. for 20–30 h. The reaction mixture was then concentrated to a volume of about 500 mL and water (600 mL) and tert-butyl methyl ether (1000 mL) were added. The MTBE layer was then separated and washed with water (500 mL). The MTBE solution was concentrated by distillation under vacuum to provide an oil and the oil was then further concentrated by distillation under high vacuum to remove excess benzylmethylamine. N-methyl-2-pyrrolidone (300 mL) was then added to the remaining oil and this solution concentrated by distillation under high vacuum to provide an oil. The oil was dissolved in MTBE (1000 mL) and the resulting solution was washed with water (2×500 mL), brine (500 mL), dried with sodium sulfate (100 g), filtered and concentrated by distillation to afford the title compound as an oil (178 g, 96% yield, >95% purity).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07183292B2
出典データセットuspto-grants-2007_02
ORD IDord-2396a5983d5a474c8730bd84baf2517b
出典メモuspto-grants-2007_02