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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475529Generated: October 26, 2026

Acetic Acid → 5-(4-(Benzyloxy)benzyl)thiazolidine-2,4-dione

https://huagongshe.com/reaction/475529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 3096180HCID 3096180—
ReactantSodium borohydrideHCID 4311764—
ReactantDimethylglyoximeHCID 135459645—
CatalystSodium HydroxideHCID 14798—
SolventWaterHCID 962—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
Product5-(4-(Benzyloxy)benzyl)thiazolidine-2,4-dioneHCID 44319268—

Reaction Conditions

Temperature0 °C

Reaction Steps

To the suspension containing CoCl2.6H2O (4.49 mg, 0.016 mmol) and dimethylglyoxime (74.54 mg, 0.64 mmol) in 10 ml of water, 4 drops of 1.0N NaOH and NaBH4 (417.1 mg, 10.85 mmol) were subsequently added. The mixture was cooled to 0° C., and 5-(4-(benzyloxy)benzylidene)thiazolidine-2,4-dione (1 g, 3.27 mmol) in 15 ml of THF-DMF (2:1) was added thereto over 20 minutes. The mixture was stirred at room temperature for 18 hours, to which acetic acid was then added until the pH thereof reached about 6. The mixture was diluted with water and extracted with ethyl acetate and water. The organic layer was washed with water several times, dried with anhydrous magnesium sulfate, filtered and solvent-evaporated. The residual oil was chromatographed on silica gel to afford 5-(4-(benzyloxy)benzyl)thiazolidine-2,4-dione (Derivative 116 of the above formula) as white solid (0.8 g, yield: 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637558B2
Source datasetuspto-grants-2014_01
ORD IDord-5aa16f9af2634ca49c29a80a16c1b3b2
Source noteuspto-grants-2014_01