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HRID 76903作成日:2026年10月25日

Diethylamine → 3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]-3-methylbutan-1-ol

https://huagongshe.com/reaction/76903

反応式

関与物質

役割名称HCID仕込み量
反応物DiethylamineHCID 8021—
反応物2-Bromobenzyl bromideHCID 76965—
反応物Sodium BicarbonateHCID 516892—
反応物1,4-Dioxane hydrochlorideHCID 20443148—
反応物4-[3-(tert-butyldimethylsilanyloxy)-1,1-dimethylpropyl]-1-trityl-1H-imidazoleHCID 53630868—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
生成物3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]-3-methylbutan-1-olHCID 58827196—

反応条件

温度80 °C

反応手順

To a solution of 4-[3-(tert-butyldimethylsilanyloxy)-1,1-dimethylpropyl]-1-trityl-1H-imidazole (650 mg, 1.27 mmol) in CH3CN (10 mL) at ambient temperature is added a solution of 2-bromobenzyl bromide (420 mg, 1.68 mmol) in CH3CN (10 mL). The resulting solution is stirred at 80° C. for 6 h. The mixture is cooled to ambient temperature and diethylamine (2 mL) is added, followed by MeOH (10 mL) and the mixture is heated at 75° C. for 1 hr and stirred at ambient temperature overnight. To the reaction mixture is added HCl/dioxane (4 M, 5 mL, 20 mmol) and stirred at ambient temperature for 1 h. The mixture is neutralized with saturated aqueous NaHCO3 and concentrated. The residue is partitioned between CH2Cl2 and brine. The organic layer is washed with brine, dried over Na2SO4 and concentrated to give an oil, which is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to yield the desired compound. MS (ESI) m/z 323 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835646B2
出典データセットuspto-grants-2014_09
ORD IDord-562c9b54bf2843f58f5b7b908d5f5023
出典メモuspto-grants-2014_09