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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380555Generated: November 1, 2026

Acetic Anhydride → HCID 13228945, compound

https://huagongshe.com/reaction/1380555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13228938HCID 13228938—
SolventPyridineHCID 1049—
ProductHCID 13228945HCID 13228945—

Reaction Steps

4-Chloro-1-(4-hydroxy-3-methylbenzyl)-2-phenylimidazole-5-acetic acid (1.1 g) was dissolved in 10 ml of pyridine, then 2 ml of acetic anhydride was added, and the mixture was stirred at room temperature for 2 hours and evaporated to dryness under reduced pressure. The residue was purified by column chromatography using 20 g of silica gel. The desired fractions were combined and evaporated to dryness under reduced pressure and the residue was recrystallized from aqueous ethanol to give 0.7 g of 4-chloro-1-(4-acetoxy-3-methylbenzyl)-2-phenylimidazole-5-acetic acid as colorless needles, m.p. 200°-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04582847
Source datasetuspto-grants-1986_04
ORD IDord-4b59e09afa08438e8925eb498aac4316
Source noteuspto-grants-1986_04