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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350822생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/350822

반응식

참여 물질

역할이름HCID투입량
반응물PhenethylamineHCID 1001—
반응물Sodium IodideHCID 5238—
반응물AcetonitrileHCID 6342—
반응물Sodium CarbonateHCID 10340—
반응물1-Octanol, 8-chloro-HCID 90012—
용매tert-Butyl methyl etherHCID 15413—
생성물8-(N-Benzyl-N-methylamino)octan-1-olHCID 1666215396%

반응 조건

온도80 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07183292B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-2396a5983d5a474c8730bd84baf2517b
출처 메모uspto-grants-2007_02