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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741342Generated: November 1, 2026

Acetic Anhydride → HCID 86751830, compound

https://huagongshe.com/reaction/1741342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 86751828HCID 86751828—
SolventPyridineHCID 1049—
ProductHCID 86751830HCID 86751830—

Reaction Steps

A mixture of 0.30 g of 5-(4-{2-[1-(3-hydroxyphenyl)ethylideneaminooxy]ethoxy}benzyl)thiazolidine-2,4-dione (prepared as described in Example 50), 0.092 ml of acetic anhydride and 15 ml of pyridine was stirred at room temperature for 1.5 hours. At the end of this time, the solvent was removed by distillation under reduced pressure, and then the resulting residue was diluted with water and then extracted with ethyl acetate. The extract was washed with 1 N aqueous hydrochloric acid and with an aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by column chromatography through silica gel, using a 1:2 by volume mixture of ethyl acetate and hexane as the eluent, to give 0.23 g of the title compound, melting at 30-50° C. (softening point).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972959
Source datasetuspto-grants-1999_10
ORD IDord-a157744d62f448118383aea4bcae22e5
Source noteuspto-grants-1999_10