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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326161Generated: October 25, 2026

Hydrochloric Acid → 5-[4-(4-Chlorobenzyloxy)benzyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/326161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantSodium hydrideHCID 24758—
Reactant5-(4-Hydroxybenzyl)thiazolidine-2,4-dioneHCID 10198397—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product5-[4-(4-Chlorobenzyloxy)benzyl]thiazolidine-2,4-dioneHCID 1294417924.4%

Reaction Steps

To 12 ml of dimethylsulfoxide is dissolved 1.12 g of 5-(4-hydroxybenzyl)thiazolidine-2,4-dione, and 480 mg of 50% sodium hydride in oil is added to the solution. The mixture is stirred at room temperature for 15 minutes, to which is added 0.81 g of 4-chlorobenzyl chloride. The whole mixture is stirred at 50° C. for 4 hours. Water is added to the mixture and the mixture is acidified with 2 N-hydrochloric acid. The mixture is subjected to extraction with ether. The extract is washed with water and dried. Ether is distilled off to give an oily substance. The oily substance is subjected to column chromatography on 30 g silica gel, elution being carried out with cyclohexane-ethyl acetate (2:1). By the above procedure there was obtained 425 mg of 5-[4-(4-chlorobenzyloxy)benzyl]thiazolidine-2,4-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04444779
Source datasetuspto-grants-1984_04
ORD IDord-d746099267f04dc89331f624dc72fad8
Source noteuspto-grants-1984_04