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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419099Generated: November 1, 2026

Acetic Anhydride → HCID 9956228, compound

https://huagongshe.com/reaction/1419099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 9867103HCID 9867103—
ProductHCID 9956228HCID 9956228—

Reaction Steps

0.032 ml of acetic anhydride were added at room temperature to a solution of 0.12 g of 5-[4-(5-hydroxy-1,4,6,7-tetramethylbenzimidazol-2-ylmethoxy)benzyl]thiazolidine-2,4-dione (prepared as described in Example 3) in 2 ml of pylidine, and the resulting mixture was stirred for 3 hours, after which it was allowed to stand overnight. At the end of this time, the reaction mixture was freed from the solvent by evaporation under reduced pressure, and the resulting residue was mixed with water. The aqueous mixture was then extracted with ethyl acetate. The extract was washed with water and then with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, after which the solid residue was triturated with diethyl ether and collected by filtration. It was then washed with diethyl ether, to give 0.12 g of the title compound, melting at 250°-253° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886014
Source datasetuspto-grants-1999_03
ORD IDord-0372216caa9f4d0a934a9cb51320ac9f
Source noteuspto-grants-1999_03