Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261090Generated: November 3, 2026

Ethylamine → 5-{[3-(Ethylamino)-4-nitrophenyl]methylidene}-1,3-thiazolidine-2,4-dione

https://huagongshe.com/reaction/2261090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant5-[(3-Fluoro-4-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dioneHCID 71378270—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-{[3-(Ethylamino)-4-nitrophenyl]methylidene}-1,3-thiazolidine-2,4-dioneHCID 71378269—

Reaction Conditions

Temperature60 °C

Reaction Steps

5-(3-Fluoro-4-nitro-benzylidene)-thiazolidine-2,4-dione (200 mg, 0.75 mmol, 1 eq.), was dissolved in DME (6 mL) and TEA (208 μL, 1.5 mmol, 2 eq.) and a solution of ethylamine (2 eq.) was added. The reaction mixture was shaken at 60° C. over night. The solvent was removed in vacuo and residue dissolved in ethyl acetate and washed with 10% ammonium chloride aqueous solution. The organic layer was dried on Na2SO4 and the solvent evaporated to give the corresponding aniline derivative as either red oil, which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846925B2
Source datasetuspto-grants-2010_12
ORD IDord-196f00412982452d81ee7473a9441538
Source noteuspto-grants-2010_12