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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1112549Erstellt: 25. Oktober 2026

Glycol monoethyl ether → HCID 178492518, Verbindung

https://huagongshe.com/reaction/1112549

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktGlycol monoethyl etherHCID 8076—
EduktSodium SulfideHCID 14804—
EduktSodiumHCID 5360545—
Edukt2,4-Diiminothiazolidinium benzenesulfonateHCID 86734211—
EduktHCID 178492520HCID 178492520—
ProduktHCID 178492518HCID 178492518—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To 140 parts of 2-ethoxyethanol stirred at 100° C. under an atmosphere of nitrogen there was added 8.6 parts of 60 percent active solid sodium sulfide and the resultant solution was filtered to remove undissolved material. The filtrate was mixed with 94 parts of dimethylformamide and 11.3 parts of 3,6-dimethoxy-phthalonitrile and the mixture stirred at 25° C. for a period of 1 hour. The reaction mixture was then heated to 95° C. over a period of 1 hour, cooled to 25° C. and filtered to remove undissolved material which was found to be (4.5 parts) unreacted 3,6-dimethoxyphthalonitrile. The filtrate, which contained approximately 0.04 mole of the sodium salt of 4,7-dimethoxy-1-imino-3-mercaptoisoindoline was stirred and there was added 10.7 parts of 2,4-diiminothiazolidinium benzenesulfonate. Stirring was continued overnight at 25° C. The product which separated was collected by filtration, washed successively with four portions of 12.0 parts each of methyl alcohol and finally dried in vacuo to obtain 4.5 parts of 4,7-dimethoxy-1-imino-3-(2,4-diimino-5-thiazolidinylidene)isoindoline as a red solid which melted at 227°-246° C. (dec).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04122261
Quelldatensatzuspto-grants-1978_10
ORD IDord-142447a1941f4ab294d3a64ef7116e27
Quellennotizuspto-grants-1978_10