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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602351Generated: November 3, 2026

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

https://huagongshe.com/reaction/1602351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl AcetateHCID 8857—
Reactant[1-(triphenylmethyl)-1H-imidazol-4-yl]methanolHCID 382182—
SolventPyridineHCID 1049—
Product(1-Trityl-1H-imidazol-4-YL)methyl acetateHCID 10762461—

Reaction Steps

Alcohol 2 (prepared above) was suspended in 500 mL of pyridine. Acetic anhydride (74 mL) was added dropwise, and the reaction was stirred for 48 hours during which it became homogeneous. The solution was poured into 2 L of EtOAc, washed with water (3×1 L), 5% aq. HCl soln. (2×1 L), sat. aq. NaHCO3, and brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide the crude product. The acetate 3 was isolated as a white powder which was sufficiently pure for use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981562
Source datasetuspto-grants-1999_11
ORD IDord-31e48fef411d46559d3994a9a46a1178
Source noteuspto-grants-1999_11