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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15413생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Ethyl AcetateHCID 8857—
반응물[1-(triphenylmethyl)-1H-imidazol-4-yl]methanolHCID 382182—
용매PyridineHCID 1049—
생성물(1-Trityl-1H-imidazol-4-YL)methyl acetateHCID 10762461—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732603B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e1e02d6c5b8641a7ae057333c534d7f7
출처 메모uspto-grants-2010_06