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Thionyl Chloride → 4-Bromothiazole-2-carbohydrazide

HRID 2091616
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2091616
[Br:1][C:2]1[N:3]=[C:4]([C:7]([OH:9])=O)[S:5][CH:6]=1.S(Cl)(Cl)=O.O.[NH2:15][NH2:16]>CO>[Br:1][C:2]1[N:3]=[C:4]([C:7]([NH:15][NH2:16])=[O:9])[S:5][CH:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 24386Thionyl ChlorideHCID 24654Hydrazine hydrate (1:1)HCID 151220654-Bromo-1,3-thiazole-2-carboxylic acid

Produkt 1

HCID 580356604-Bromothiazole-2-carbohydrazideAusbeute 78,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 4-bromothiazole-2-carboxylic acid (2.0 g, 9.8 mmol) in methanol (10 mL) was added thionyl chloride (710 μL, 9.8 mmol) and the mixture was refluxed for 3 hours. The solvent was removed under reduced pressure, and the residue was suspended in ethanol (10 mL). To this suspension was added hydrazine hydrate (2.4 mL, 49 mmol), and the reaction was heated to reflux for 90 minutes. The solvent was removed under reduced pressure, and the residue suspended in acetonitrile, filtered, and the solids were washed with acetonitrile, diethyl ether, and dried under vacuum to afford 1.7 g (77%) of 4-bromothiazole-2-carbohydrazide as a yellow solid. M+1=222.1

Aufarbeitung

  1. temperaturethe mixture was refluxed for 3 hours
  2. customThe solvent was removed under reduced pressure
  3. temperaturethe reaction was heated
  4. temperatureto reflux for 90 minutes
  5. customThe solvent was removed under reduced pressure
  6. filtrationfiltered
  7. washthe solids were washed with acetonitrile, diethyl ether
  8. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-0ef677d8434c454d99fad4f728dd63e6
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08440665B2

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