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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37655생성일: 2026년 10월 24일

Hydrogen Bromide → 3-(Methyl(3-phenylpropyl)amino)-5-hydroxychroman

https://huagongshe.com/ko/reaction/37655

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물FormaldehydeHCID 712—
반응물BenzenepropanalHCID 7707—
반응물Sodium HydroxideHCID 14798—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물5-Methoxy-3,4-dihydro-2H-1-benzopyran-3-amineHCID 13928948—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물3-(Methyl(3-phenylpropyl)amino)-5-hydroxychromanHCID 19028156—

반응 조건

온도0 °C

반응 단계

3-Amino-5-methoxychroman (Thorberg et al. Acta Pharm. Suec. 24(1987)) (2.0 g, 9.28 mmol) was dissolved in methanol (50 ml) and pH was adjusted to 6.0 with acetic acid. The solution was cooled to 0° C. and sodium cyanoborohydrid (0.87 g, 13.8 mmol) was added together with 3-phenylpropanal (1.22 ml, 9.28 mmol), the cooling was withdrawn and the solution was stirred at ambient temperature for 4 hours. Paraformaldehyde (0.42 g, 14 mmol) and sodium cyanoborohydride (0.87 g, 9.28 mmol) was added and stirring was continued overnight at ambient temperature. The solution was diluted with toluene and washed with water. Drying with sodium sulfate and evaporation to dryness gives an oil. The oil was purified by flash chromatography on silica gel by elution with ethylacete/hexane 1:4. The collected fractions were evaporated to give an oil. The oil was treated with HBr (47% aq.) at 120° C. for 1 hour. The solution was cooled and neutralised with sodium hydroxide and extracted with toluene. The organic phase was dried and evaporated to give the title compound as an oil. 13C-NMR: 22.502 29.09 33.47 38.19 53.66 67.75 102.04 109.20 110.46 125.78 127.05 128.36 142.20 155.29 158.28.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420151
출처 데이터셋uspto-grants-1995_05
ORD IDord-256a891971184aa7b2d20ad7b29aba8d
출처 메모uspto-grants-1995_05