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HRID 1267679作成日:2026年10月26日

N,N-Dimethylaniline → Resveratrol

https://huagongshe.com/reaction/1267679

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylanilineHCID 949—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物(E)-3,5,4'-TribenzyloxystilbeneHCID 10217778—
溶媒DichloromethaneHCID 6344—
生成物ResveratrolHCID 445154—

反応条件

温度45 °C

反応手順

In a 3 lit. round-bottomed flask equipped with a thermometer are added aluminum chloride (390.35 gm) and N, N-dimethylaniline (413.10 gm) maintaining the temperature at 40-50° C.(exothermic). To this solution, (E)-1-[4-(benzyloxy)phenyl]-2-[3,5-bis(benzyloxy)phenyl]ethene (243 gm) in dichloromethane (800 ml) is added and stirred for further 0.75 hour. After the reaction is over, the reaction mixture is quenched into dil. hydrochloric acid at 0-5° C. and extracted with ethyl acetate. The organic layer is charcoalized and concentrated to get pure (E)-1-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)ethene (trans-Resveratrol) in the exclusive trans form. Mp 257-259° C. 1H NMR (DMSO-d6, 400 MHz) δ 6.11 (t, J=1.8 Hz, 1H), 6.38(d, J=1.8 Hz, 2H), 6.75 (d, J=8.5 Hz, 2H), 6.82(d, J=16.3 Hz, 1H), 6.92(d, J=16.3, 1H), 7.39(d, J=8.4 Hz, 2H); Mass M/e:228.2

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06552213B1
出典データセットuspto-grants-2003_04
ORD IDord-1fbfab3fe1fa4d9b8bdd9c920fdc18e2
出典メモuspto-grants-2003_04