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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981925Generated: October 28, 2026

Acetic Anhydride → HCID 13556431, compound

https://huagongshe.com/reaction/1981925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSelenazofurinHCID 100665—
ProductHCID 13556431HCID 13556431—

Reaction Steps

A mixture of 2-β-D-ribofuranosylselenazole-4-carboxamide (1.0 g, 3.25 mmol), N,N-dimethylaminopyridine (catalyst, 80 mg) and acetic anhydride (15 ml) was stirred at room temperature for 3 hours. The solvent was evaporated in vacuo and coevaporated with water (10 ml×2) to provide COMPOUND 3 as a white crystalline product which was triturated with water and collected by filtration. The product was recrystallized from water containing a few drops of ethanol to provide white needles: yield 1.2 g (85 percent), mp 117-119 degrees C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04594414
Source datasetuspto-grants-1986_06
ORD IDord-157c1eb09c2a4193814abbfad2622b41
Source noteuspto-grants-1986_06