StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Tetrahydrofuran → 5-Methylsulfonyltetrazole

HRID 2193835
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2193835
CS[C:3]1[NH:7][N:6]=[N:5][N:4]=1.[S:8]([O-:13])(O[O-])(=O)=[O:9].[K+].[K+].[CH2:16]1COCC1>O>[CH3:16][S:8]([C:3]1[NH:7][N:6]=[N:5][N:4]=1)(=[O:13])=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8028TetrahydrofuranHCID 10313463Potassium peroxymonosulphateHCID 178503621HCID 178503621, Verbindung

Produkt 1

HCID 1785048625-Methylsulfonyltetrazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To a stirred solution of 5-(methylthio)-1H-tetrazole (300 mg; Aldrich Chemical Company, Inc., Milwaukee, Wis.) in THF (15 mL) and water (15 mL) was added potassium peroxomonosulfate (Oxone®, DuPont Specialty Chemicals, Deepwater, N.J., USA) (3.18 g). After stirring at room temperature for five days, the reaction mixture was filtered and the filtercake was washed with THF. The filtrate was concentrated under reduced pressure. Crude NMR showed this to be a mixture of desired product and starting material, so the mixture was taken up in methanol and treated with potassium peroxomonosulfate (Oxone®, DuPont Specialty Chemicals, Deepwater, N.J., USA). After stirring at room temperature for five days, the reaction mixture was filtered and the filtercake was washed with methanol. The filtrate was concentrated under reduced pressure to afford 0.400 g of impure (I-11a) as a solid which was used in the next step without purification; m/z 146.9 (M−H)−.

Aufarbeitung

  1. filtrationthe reaction mixture was filtered
  2. washthe filtercake was washed with THF
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. additiona mixture of desired product
  5. additiontreated with potassium peroxomonosulfate (Oxone®, DuPont Specialty Chemicals, Deepwater, N.J., USA)
  6. stirringAfter stirring at room temperature for five days
  7. filtrationthe reaction mixture was filtered
  8. washthe filtercake was washed with methanol
  9. concentrationThe filtrate was concentrated under reduced pressure
  10. customto afford 0.400 g of impure (I-11a) as a solid which
  11. customwas used in the next step without purification

Quellen und Nachweise

ORD-Eintrag
ord-923f2d8ef9844d19a944a28c730aaa63
Quelldatensatz
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08329920B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion