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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394391Generated: November 3, 2026

Ethanol → HCID 54151686, compound

https://huagongshe.com/reaction/2394391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
ReactantHCID 17221112HCID 17221112—
SolventDiethyl EtherHCID 3283—
ProductHCID 54151686HCID 5415168676%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 60 ml of ethanol, there were dissolved 3.00 g of 1-benzylindole-4-carbaldehyde prepared in Example 1 and 0.22 g of piperidine, followed by addition of 2.99 g of 2,4-thiazolidinedione to the resulting solution and heating the mixture under reflux for 24 hours. To the reaction solution, there was added 120 ml of diethyl ether and the mixture was stirred at 0° C. for one hour. The crystals precipitated were filtered off and washed with a diethyl ether/ethanol (2:1) mixed solvent. The crystals were dried under reduced pressure to give 3.24 g of 5-(1-benzylindol-4-yl)methylene-2,4-thiazolidinedione as yellow crystals. The yield thereof was found to be 76%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811439
Source datasetuspto-grants-1998_09
ORD IDord-c4b5f6acd22849d1bbcfc630c8ccd160
Source noteuspto-grants-1998_09