戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 37655作成日:2026年10月25日

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

https://huagongshe.com/reaction/37655

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物FormaldehydeHCID 712—
反応物BenzenepropanalHCID 7707—
反応物Sodium HydroxideHCID 14798—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物5-Methoxy-3,4-dihydro-2H-1-benzopyran-3-amineHCID 13928948—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
生成物3-(Methyl(3-phenylpropyl)amino)-5-hydroxychromanHCID 19028156—

反応条件

温度0 °C

反応手順

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cyanoborohydrid (0.87 g, 13.8 mmol) was added together with 3-phenylpropanal (1.22 ml, 9.28 mmol), the cooling was withdrawn and the solution was stirred at ambient temperature for 4 hours.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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420151
出典データセットuspto-grants-1995_05
ORD IDord-256a891971184aa7b2d20ad7b29aba8d
出典メモuspto-grants-1995_05