Water → HCID 178508738, Verbindung

HRID 1730780Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1730780
[OH-].[NH4+].O.C1(S([O-])(=O)=O)C=CC=CC=1.[NH:14]=[C:15]1[NH2+:19][C:18](=[NH:20])[CH2:17][S:16]1.[NH:21]=[C:22]1[C:30]2[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:24](=N)[NH:23]1>CO>[NH:21]=[C:22]1[C:30]2[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:24](=[C:17]2[S:16][C:15](=[NH:14])[NH:19][C:18]2=[NH:20])[NH:23]1

Komponenten

6

Versuchsvorschrift

To a stirred solution of 61 parts of 28 percent aqueous ammonium hydroxide solution and 2500 parts of water under at 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 finely 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.).

Aufarbeitung

  1. customA yellow solid separated during the addition
  2. waitwas continued at room temperature for approximately sixteen hours
  3. filtrationthe thick yellow reaction slurry was then filtered
  4. customThe product collected on the funnel
  5. washwas washed copiously with distilled water
  6. customfinely dried at 50° C in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-fc4e57d6c8f14eac9f4ca59e4ee34500
Quelldatensatz
uspto-grants-1976_11
Patentnummer
US03993658

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