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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 921040Erstellt: 25. Oktober 2026

Carbon Dioxide → HCID 67995414, Verbindung

https://huagongshe.com/reaction/921040

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktSodium CarbonateHCID 10340—
Edukt1,2-Phenylenediamine dihydrochlorideHCID 11990—
Edukt2-(Tert-butyl)pyrimidine-5-carbonitrileHCID 817771—
Edukt3,4-Diamino-6-tert-butylpyridine dihydrochlorideHCID 67995003—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktHCID 67995414HCID 67995414—

Reaktionsschritte

Preparation analogous to 16), S43, using 16.1 g (100 mmol) of 2-tert-butyl-5-cyanopyrimidine [126230-72-6] and 71.4 g (300 mmol) of 3,4-diamino-6-tert-butylpyridine dihydrochloride (S50) instead of 25.9 g (100 mmol) of 2-N-pivaloylamido-3-cyano-6-tert-butylpyridine (S42) and 90.5 g (500 mmol) of o-phenylenediamine dihydrochloride [615-28-1]. After cooling, the violet melt is dissolved in a mixture of 150 ml of ethanol and 300 ml of water at elevated temperature, and a solution of 25 g of sodium carbonate in 100 ml of water is then added dropwise with vigorous stirring (note: foaming, evolution of carbon dioxide). When the addition is complete, the mixture is stirred for a further 30 min., the brown solid is then filtered off with suction, washed three times with 100 ml of water each time and dried in vacuo. Yield: 23.8 g (77 mmol), 77%. Purity: >95% according to 1H-NMR.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09273080B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-5e49d604c9bd434f8499cee66314e496
Quellennotizuspto-grants-2016_03