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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833498Generated: October 26, 2026

Water → HCID 178508738, compound

https://huagongshe.com/reaction/1833498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium HydroxideHCID 14923—
Reactant2,4-Diiminothiazolidinium benzenesulfonateHCID 86734211—
ReactantHCID 178508669HCID 178508669—
SolventMethanolHCID 887—
ProductHCID 178508738HCID 178508738—

Reaction Steps

To a stirred solution of 61 parts of 28 percent aqueous ammonium hydroxide solution and 2500 parts of water under an atmosphere of nitrogen there was simultaneously added at ambient temperature during a period of ninety minutes 273 parts of 2,4-diiminothiazolidinium benzenesulfonate and 853 parts of a 17.1 percent by weight methyl alcohol solution of 1,3-diiminoisoindoline. A yellow solid separated during the addition. Stirring was continued at room temperature for approximately sixteen hours after the additions were complete and the thick yellow reaction slurry was then filtered. The product collected on the funnel was washed copiously with distilled water and finally dried at 50° C in vacuo to obtain 233 parts of 1-imino-3-(2,4-diimino-5-thiazolidinylidene)isoindoline as a yellow solid melting at 252°-263° C (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066653
Source datasetuspto-grants-1978_01
ORD IDord-20e7cb71dd694ffc9552438bc7865f30
Source noteuspto-grants-1978_01