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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418428Generated: November 3, 2026

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

https://huagongshe.com/reaction/1418428

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

The alcohol from Step B (260 mmol, prepared above) was suspended in pyridine (500 mL). Acetic anhydride (74 mL, 780 mmol) was added dropwise, and the reaction was stirred for 48 hours during which it became homogeneous. The solution was poured into EtOAc, washed sequentially with water, 5% aq. HCl solution, sat. aq. NaHCO3, solution, and brine. The organic extracts were dried, (Na2SO4), and concentrated in vacuo to provide the product as a white powder, which was sufficiently pure for use in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883105
Source datasetuspto-grants-1999_03
ORD IDord-9e66b3a284b2415c87223614d11ce3b5
Source noteuspto-grants-1999_03