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Tetrahydrofuran → 5-Methylsulfonyltetrazole

HRID 1942324
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1942324
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
  11. customa solid which was used in the next step without purification

Quellen und Nachweise

ORD-Eintrag
ord-9f26e387237440c6ba49cf9e61937f0c
Quelldatensatz
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08389552B2

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