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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217785생성일: 2026년 10월 26일

3-Methoxypropylamine → 3-(4-bromophenyl)-N-(3-methoxypropyl)propan-1-amine

https://huagongshe.com/reaction/217785

반응식

참여 물질

역할이름HCID투입량
반응물3-MethoxypropylamineHCID 1672—
반응물Potassium CarbonateHCID 11430—
반응물3-(4-Bromophenyl)propyl methanesulphonateHCID 19688466—
용매AcetonitrileHCID 6342—
생성물3-(4-bromophenyl)-N-(3-methoxypropyl)propan-1-amineHCID 66678580—

반응 조건

온도85 °C

반응 단계

3-(4-bromophenyl)propyl methanesulfonate (418 g) and acetonitrile (2 L) were charged into reactor 1. 3-methoxypropylamine (305 g) and potassium carbonate (394 g) were added to reactor 1 and the mixture was warmed to 80-90° C. for 4-16 h. The mixture was analysed for completion (3-(4-bromophenyl)propyl methanesulfonate <0.5%). The reaction was cooled to 25° C. and the suspension was filtered to remove the white solids. The filtrate was concentrated to dryness on a rotary evaporator. The crude product from the rotary evaporator, MTBE (2 L) and water (1.5 L) were charged into reactor 2. After phase separation, the organic layer was collected and washed with 1N HCl (2 L) until pH=4-5. After phase separation, the aqueous phase was basified by 2.5N NaOH solution to pH=9-10 and the resulting aqueous solution was used in the next step without further treatment.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198285B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a183de74b8264e66a58fed0d0b7f9435
출처 메모uspto-grants-2012_06