Dimethylformamide → 1-(2-Methyl-3-methylsulfanylphenyl)-4-methyl-1,4-dihydrotetrazole-5-one

HRID 628502Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 628502
[CH3:1][C:2]1[C:7]([S:8][Si](C(C)C)(C(C)C)C(C)C)=[CH:6][CH:5]=[CH:4][C:3]=1[N:19]1[C:23](=[O:24])[N:22]([CH3:25])[N:21]=[N:20]1.[F-].[Cs+].[CH3:28]N(C)C=O.CI>O>[CH3:1][C:2]1[C:7]([S:8][CH3:28])=[CH:6][CH:5]=[CH:4][C:3]=1[N:19]1[C:23](=[O:24])[N:22]([CH3:25])[N:21]=[N:20]1

Komponenten

6

Versuchsvorschrift

A mixture of 1-(2-methyl-3-triisopropylsilanylsulfanylphenyl)-4-methyl-1,4-dihydrotetrazole-5-one 3.63 g, cesium fluoride 2.91 g and N,N-dimethylformamide 10 ml was stirred at room temperature for thirty minutes. To the resulting mixture was added methyl iodide 2.72 g and the resulting mixture was stirred at room temperature for three hours. To the reaction mixture was added water and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated saline, and was dried over anhydrous magnesium sulfate and was then concentrated under reduced pressure. The resulting residue was subjected to a silica gel column chromatography to give 1-(2-methyl-3-methylthiophenyl)-4-methyl-1,4-dihydrotetrazole-5-one 1.65 g.

Aufarbeitung

  1. stirringthe resulting mixture was stirred at room temperature for three hours
  2. extractionthe resulting mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with water and saturated saline
  4. dry with materialwas dried over anhydrous magnesium sulfate
  5. concentrationwas then concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-70463f43b9f247f69a49adc5096719a5
Quelldatensatz
uspto-grants-2016_04
Patentnummer
US09314023B2

Notizen zur Reaktion

Wird geladen…