戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1269346作成日:2026年10月25日

Imidazole → (2Z)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-en-1-ol

https://huagongshe.com/reaction/1269346

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物(2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diolHCID 57434773—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物(2Z)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-en-1-olHCID 5878778217.5%

反応条件

温度-78 °C

反応手順

To a solution of 110 g of (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol and 50 g of imidazole in 1 L of THF stirred at −78° C., a solution 51 g of TBSCl in 250 mL of dichloromethane was added dropwise. The resulting mixture was stirred at −78° C. 0.5 hr. Brine was then added and then warmed to room temperature. The organic phase was separated and the aqueous phase was extracted with EtOAc. The organic phases were combined and dried over Na2SO4 and evaporated. The resulting crude material was purified by flash chromatography to afford 25.6 g of the title compound as a white solid. 1H NMR (acetone-d6, 500 M Hz): δ 7.69 (d, 2 H), 7.37 (d, 2 H), 7.18–7.04 (m, 5 H), 4,77 (s, 2 H), 4.65 (d, 2 H), 3.96 (t, 1H, OH), 3.03 (s, 3 H), 0.84 (s, 9 H), 0.01 (s, 6 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07199154B2
出典データセットuspto-grants-2007_04
ORD IDord-bbfc37b0d2ed4f2a81fb6580611a58cd
出典メモuspto-grants-2007_04