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HRID 15413作成日:2026年10月23日

Acetic Anhydride → (1-Trityl-1H-imidazol-4-YL)methyl acetate

https://huagongshe.com/ja/reaction/15413

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Ethyl AcetateHCID 8857—
反応物[1-(triphenylmethyl)-1H-imidazol-4-yl]methanolHCID 382182—
溶媒PyridineHCID 1049—
生成物(1-Trityl-1H-imidazol-4-YL)methyl acetateHCID 10762461—

反応手順

To a suspension of the title A compound 1-trityl-4-hydroxymethyl-1H-imidazole (34.5 g, 101 mmol) in pyridine (200 mL) is added acetic anhydride (28.6 mL, 303 mmol) in a dropwise fashion and the reaction is stirred until it becomes clear. The reaction mixture is poured into EtOAc and then washed with 0.5N aqueous HCl, saturated aqueous sodium bicarbonate and brine. The combined organic phases are dried over anhydrous sodium sulfate and then filtered through a silica pad yielding a solid after removal of the solvent in vacuo. The solid is triturated with diethyl ether to give 4-acetoxymethyl-1-tritylimidazole: m.p. 133-134° C.; 1H-NMR (DMSO-d6) δ 7.42 (10H, m), 7.09 (6H, m), 6.99 (1H, s), 4.89 (2H, s), 1.99 (3H, s); e/z (ES) 383 (M+1, 5%), 243 (100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732603B2
出典データセットuspto-grants-2010_06
ORD IDord-e1e02d6c5b8641a7ae057333c534d7f7
出典メモuspto-grants-2010_06