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HRID 465868作成日:2026年10月26日

Imidazole → 2-[2-[[Dimethyl(1,1,2-trimethylpropyl)silyl]oxy]ethyl]benzene bromide

https://huagongshe.com/reaction/465868

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物Dimethylthexylsilyl chlorideHCID 144239—
反応物2-(2-Bromophenyl)ethan-1-olHCID 2734089—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物2-[2-[[Dimethyl(1,1,2-trimethylpropyl)silyl]oxy]ethyl]benzene bromideHCID 19875376—

反応条件

温度0 °C

反応手順

2-Bromophenethyl alcohol (43.80 g, 217.9 mmol) was dissolved in anhydrous CH2Cl2 (200 mL) and imidazole (16.32 g, 239.6 mmol) was added and stirred under argon 0° C. Dimethylthexylsilyl chloride (42.83 g, 239.6 mmol) was added dropwise and the reaction mixture was stirred for three days at room temperature. It was diluted with H2O (50 mL) and ether (100 mL) and partitioned. The aqueous layer was extracted with ether (2×100 mL). The combined organic layers were washed with 5% aqueous HCl (1 time), H2O (1 time), aqueous NaHCO3 (1 time), H2O (1 time), and brine, then dried (MgSO4) and concentrated in vacuo to obtain a yellow oil. The crude product was Kugelrohr distilled (55°-80° ) under oil pump vacuum to give the purified title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05153327
出典データセットuspto-grants-1992_10
ORD IDord-a0c538e554cc4726895b1e987c7f877d
出典メモuspto-grants-1992_10