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HRID 1042600作成日:2026年10月27日

3,4,5-Trimethoxybenzaldehyde → 3-(2-Furyl)-1-(3,4,5-trimethoxyphenyl)prop-2-yn-1-one

https://huagongshe.com/reaction/1042600

反応式

関与物質

役割名称HCID仕込み量
反応物3,4,5-TrimethoxybenzaldehydeHCID 6858—
反応物Furan, 2-ethynyl-HCID 140409—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-Furyl)-1-(3,4,5-trimethoxyphenyl)prop-2-yn-1-oneHCID 57421963—

反応条件

温度-78 °C

反応手順

2-Ethynylfuran (200 mg, 2.17 mmol) was dissolved in dry THF (10 ml) and cooled to −78° C. under N2 atmosphere. BuLi (1.2 ml, 2.4 mmol) was added slowly and stirred at −78° C. for 10 min and then 3,4,5-trimethoxybenzaldehyde (500 mg, 2.6 mmol) was added and reaction mixture was stirred for 1 h at −78° C. and then reaction temp raised to room temp. The reaction was quenched by addition of aqueous NH4Cl solution and extracted with EtOAc. The colorless oil was dissolved in dichloromethane and excess of MnO2 was added to it and stirred overnight at room temp. The reaction mixture was filtered through celite plug and evaporated to dryness. 3-(2-furyl)-1-(3,4,5-trimethoxyphenyl)prop-2-yn-1-one was precipitated from ether by slow addition of hexane as off-white powder (65%). 1H NMR (300 MHz, CDCl3) δ 3.93 (s, 9H), 6.50-6.52 (m, 1H), 7.01 (d, J=3.6 Hz, 1H), 7.45 (s, 2H), 7.24 (s, 1H), 7.55 (d, J=1.5 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08557982B2
出典データセットuspto-grants-2013_10
ORD IDord-077b0e23ea9b4bdd83fed3acfe65f9a4
出典メモuspto-grants-2013_10