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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436858Generated: October 25, 2026

2-Thiazolidinone,4-thioxo- → HCID 178508330, compound

https://huagongshe.com/reaction/436858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiazolidinone,4-thioxo-HCID 1539595—
ReactantHCID 178508669HCID 178508669—
SolventMethanolHCID 887—
ProductHCID 178508330HCID 178508330—

Reaction Steps

To a stirred solution of 49.7 parts of 2-oxo-4-thioxothiazolidine in 990 parts of methanol there was added at 40° C. and under an atmosphere of nitrogen 54.3 parts of powdered 1,3-diiminoisoindoline. Initially, a thick slurry resulted. The reaction mixture was stirred at room temperature for two hours during which time the mixture gradually thinned. The mixture was then heated at reflux for approximately two hours and after cooling to 25° C., was filtered. The collected solid was washed with fresh methanol and dried in vacuo at 50° C. to obtain 1-imino-3-(2-oxo-4-thioxo-5-thiazolidinylidene)isoindoline as an orange powder melting at 267°-8° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04028372
Source datasetuspto-grants-1977_06
ORD IDord-22216317c05d493e81fdc0e0761e14fe
Source noteuspto-grants-1977_06