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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15413Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktEthyl AcetateHCID 8857—
Edukt[1-(triphenylmethyl)-1H-imidazol-4-yl]methanolHCID 382182—
LösungsmittelPyridineHCID 1049—
Produkt(1-Trityl-1H-imidazol-4-YL)methyl acetateHCID 10762461—

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732603B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-e1e02d6c5b8641a7ae057333c534d7f7
Quellennotizuspto-grants-2010_06