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1-Bromohexane → Sbb043676

HRID 1073787
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1073787
[NH2:1][C:2]1[S:3][C:4]([SH:7])=[N:5][N:6]=1.[OH-].[Na+].Br[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>C(O)C.O>[NH2:1][C:2]1[S:3][C:4]([S:7][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[N:5][N:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 81011-BromohexaneHCID 14798Sodium HydroxideHCID 178509208HCID 178509208, Verbindung

Produkt 1

HCID 1579472Sbb043676Ausbeute 77,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel2×

Versuchsvorschrift

In 190 ml of ethanol and 240 ml of water, 81.5 g of 2-amino-5-mercapto-1,3,4-thiadiazole and 26.9 g of sodium hydroxide were added. To this solution, 99 g of 1-bromohexane was added and the resulting mixture was warmed to 60°~70° C. and stirred for 2 hours. After cooling, water was added to the reaction mixture, and the resulting solution was filtered. The residue was washed with water and dried under reduced pressure. The dried residue was recrystallized from an ethanol/hexane mixture, and thus 100.5 g of 2-amino-5-hexylthio-1,3,4-thiadiazole was obtained. m.p. 113°~115° C. Yield 77%.

Aufarbeitung

  1. temperaturethe resulting mixture was warmed to 60°~70° C.
  2. temperatureAfter cooling
  3. filtrationthe resulting solution was filtered
  4. washThe residue was washed with water
  5. customdried under reduced pressure
  6. customThe dried residue was recrystallized from an ethanol/hexane mixture

Quellen und Nachweise

ORD-Eintrag
ord-5267acc46329413ca55d2359d49b20ee
Quelldatensatz
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04971971

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