HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15413Generated: October 23, 2026
Acetic Anhydride → (1-Trityl-1H-imidazol-4-YL)methyl acetate
https://huagongshe.com/en/reaction/15413
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | [1-(triphenylmethyl)-1H-imidazol-4-yl]methanol | HCID 382182 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (1-Trityl-1H-imidazol-4-YL)methyl acetate | HCID 10762461 | — |
Reaction Steps
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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732603B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-e1e02d6c5b8641a7ae057333c534d7f7 |
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| Source note | uspto-grants-2010_06 |
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