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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30645Generated: October 25, 2026

3-Methyl-5-[(4-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dione → 5-(4-Aminobenzyl)-3-methyl-1,3-thiazolane-2,4-dione

https://huagongshe.com/reaction/30645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-5-[(4-nitrophenyl)methylidene]-1,3-thiazolidine-2,4-dioneHCID 1482884—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
Product5-(4-Aminobenzyl)-3-methyl-1,3-thiazolane-2,4-dioneHCID 276837379.4%

Reaction Steps

A mixture of 3-methyl-5-(4-nitrobenzylidene)-1,3-thiazolidine-2,4-dione (1.0 g), 5% palladium carbon (1.0 g) and tetrahydrofuran (150 mL) was subjected to catalytic reduction under hydrogen pressure of 5.0 kgf·cm−2. The catalyst was removed by filtration, and the filtrate was concentrated to give 5-(4-aminobenzyl)-3-methyl-1,3-thiazolidine-2,4-dione as colorless crystals (0.71 g, yield 79%). Recrystallization thereof from ethyl acetate-hexane gave colorless prism crystals. melting point: 91-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423159B2
Source datasetuspto-grants-2008_09
ORD IDord-45c08b9c0289483abe2788e113b3c415
Source noteuspto-grants-2008_09