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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399135Generated: October 30, 2026

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

https://huagongshe.com/reaction/399135

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

1-Triphenylmethyl-4-(hydroxymethyl)-imidazole (260 mmol) was suspended in pyridine (500 mL). Acetic anhydride (74 mL, 780 mmol) was added dropwise, and the reaction was stirred for 48 hr during which it became homogeneous. The solution was poured into EtOAc, washed sequentially with water, 5% aqueous HCl solution, satd aqueous 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 numberUS05817678
Source datasetuspto-grants-1998_10
ORD IDord-3add961944cc4fe99646873fa67f031c
Source noteuspto-grants-1998_10