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HRID 55932作成日:2026年10月24日

Dimethyl Sulfone → 1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethenamine

https://huagongshe.com/ja/reaction/55932

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoneHCID 6213—
反応物HexaneHCID 8058—
反応物3-Ethoxy-4-methoxybenzonitrileHCID 3934769—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethenamineHCID 8669381983.4%

反応条件

温度27.5 °C

反応手順

A slurry of dimethylsulfone (85 g, 903 mmol) in THF (480 ml) was treated with a 1.6M solution of n-butyllithium in hexane (505 ml, 808 mmol) at 0-5° C. The resulting mixture was agitated for 1 hour then a solution of 3-ethoxy-4-methoxybenzonitrile (80 g, 451 mmol) in THF (240 ml) was added at 0-5° C. The mixture was agitated at 0-5° C. for 0.5 hour, warmed to 25-30° C. over 0.5 hour and then agitated for 1 hour. Water (1.4 L) was added at 25-30° C. and the reaction mass was agitated overnight at room temperature (20-30° C.). The solid was filtered and subsequently washed with a 2:1 mixture of water:THF (200 ml), water (200 ml) and heptane (2×200 ml). The solid was dried under reduced pressure at 40-45° C. to provide the product as a white solid (102 g, 83% yield); 1H NMR (DMSO-d6) δ 1.34 (t, J=7.0 Hz, 3H), 2.99 (s, 3H), 3.80 (s, 3H), 4.08 (q, J=7.0 Hz, 2H), 5.03 (s, 1H), 6.82 (s, 2H), 7.01 (d, J=8.5 Hz, 1H), 7.09-7.22 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434689B2
出典データセットuspto-grants-2016_09
ORD IDord-f3357c3e07c34d3ba3fecb7c78a96830
出典メモuspto-grants-2016_09