戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 76892作成日:2026年10月24日

2-Bromobenzyl bromide → 3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]propionic acid methyl ester

https://huagongshe.com/ja/reaction/76892

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromobenzyl bromideHCID 76965—
反応物Methyl 3-(1-Tritylimidazol-4-yl) PropionateHCID 10475868—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]propionic acid methyl esterHCID 58827130—

反応手順

To a solution of 3-(1-trityl-1H-imidazol-4-yl)propanoic acid methyl ester (5.0 g, 12.6 mmol) in CH3CN (80 mL) is added a solution of 2-bromobenzylbromide (2.84 g, 11.4 mmol) in CH3CN (20 mL). The resulting clear solution is stirred at ambient temperature over the weekend. The mixture is concentrated and the remaining oil is taken up in 85 mL methanol and heated up at 70° C. for 2 h. Then the mixture is concentrated to give a yellow oil, which is taken up in EtOAc and washed with saturated aqueous NaHCO3 and brine, dried over anhydrous Na2SO4, and concentrated to yield a viscous oil. The crude reaction mixture is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to give 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-b41e2132a9a845cb9b032efa260435e5
出典メモuspto-grants-2014_09