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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956941Generated: November 1, 2026

Acetophenone → 5-{4-[2-(1-Phenylethylideneaminooxy)ethoxy]benzyl}thiazolidine-2,4-dione

https://huagongshe.com/reaction/1956941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
Reactant5-(4-[2-Aminooxyethoxy)benzyl]thiazolidine-2,4-dione hydrochlorideHCID 21833965—
Product5-{4-[2-(1-Phenylethylideneaminooxy)ethoxy]benzyl}thiazolidine-2,4-dioneHCID 73847991—

Reaction Steps

Following a procedure similar to that described in Example 40(f), 0.16 ml of acetophenone was reacted with 400 mg of 5-[4-(2-aminooxyethoxy)benzyl]thiazolidine-2,4-dione hydrochloride [prepared as described in Example 40(e)]. The reaction mixture was then concentrated by evaporation under reduced pressure, and the resulting residue was extracted with ethyl acetate. The extract was washed with water and the solvent was removed by distillation under reduced pressure. The residue was mixed with diisopropyl ether and the mixture was stirred. The precipitated powder was collected by filtration, to give 370 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780490
Source datasetuspto-grants-1998_07
ORD IDord-ae1012f7ddf54c7c9bf8cfbef321aa3d
Source noteuspto-grants-1998_07