Potassium Carbonate → 1-Phenyl-5-(5-trifluoromethyl-thiophen-3-yloxy)-1H-tetrazole

HRID 1297177

Reaktionsgleichung

Reaktionsgleichung von HRID 1297177
[F:1][C:2]([F:10])([F:9])[C:3]1[S:7][CH:6]=[C:5]([OH:8])[CH:4]=1.Cl[C:12]1[N:16]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[N:15]=[N:14][N:13]=1.C([O-])([O-])=O.[K+].[K+]>CC(C)=O>[C:17]1([N:16]2[C:12]([O:8][C:5]3[CH:4]=[C:3]([C:2]([F:10])([F:9])[F:1])[S:7][CH:6]=3)=[N:13][N:14]=[N:15]2)[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Komponenten

5

Versuchsvorschrift

A solution of 5-trifluoromethyl-thiophen-3-ol (2.0 g, 11.9 mmol) in dry acetone (480 mL) containing 5-chloro-1-phenyl-1H-tetrazole (2.1 g, 11.9 mmol) and K2CO3 (3.3 g, 23.8 mmol) is maintained at reflux with careful exclusion of moisture overnight. The acetone is removed under reduced pressure and the residue is partitioned between CH2Cl2 (500 mL) and H2O (50 mL). The organic extracts are washed with brine, then dried (Na2SO4), filtered and concentrated. The crude product is chromatographed on silica gel, eluting with EtOAc:Hex (1:80) to afford the title compound (2.5 g, 68%) as a white solid.

Aufarbeitung

  1. temperatureis maintained
  2. temperatureat reflux with careful exclusion of moisture overnight
  3. customThe acetone is removed under reduced pressure
  4. customthe residue is partitioned between CH2Cl2 (500 mL) and H2O (50 mL)
  5. washThe organic extracts are washed with brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe crude product is chromatographed on silica gel
  10. washeluting with EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-4789db7cde8d4731a0970eae3c6b9bdf
Quelldatensatz
uspto-grants-2007_07
Patentnummer
US07250430B2

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