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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741327Generated: November 1, 2026

Hydrazine hydrate (1:1) → 5-[4-(2-Aminooxyethoxy)benzyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/1741327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 21834037HCID 21834037—
SolventEthanolHCID 702—
Product5-[4-(2-Aminooxyethoxy)benzyl]thiazolidine-2,4-dioneHCID 21833966106.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

0.32 ml of hydrazine monohydrate was added to a suspension of 2.64 g of 5-[4-(2-phthalimidooxyethoxy)-benzyl]thiazolidine-2,4-dione [prepared as described in step (d) above] in 30 ml of ethanol, and the resulting mixture was stirred at 80° C. for 2 hours. At the end of this time, the reaction mixture was cooled and the precipitated phthalhydrazide was filtered off. The filtrate was concentrated by evaporation under reduced pressure, and the concentrate was purified by column chromatography through silica gel, using a 1:20 by volume mixture of methanol and methylene chloride as the eluent, to give 1.93 g of 5-[4-(2-aminooxyethoxy)benzyl]-thiazolidine-2,4-dione as a syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972959
Source datasetuspto-grants-1999_10
ORD IDord-e50381e8764848e8973b9fae0b2b0ba7
Source noteuspto-grants-1999_10