Sodium Iodide → 5-Iodomethyl-1-methyl-3-(4-trifluoromethoxy-phenyl)-1H-pyrazole

HRID 915470Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 915470
Cl[CH2:2][C:3]1[N:7]([CH3:8])[N:6]=[C:5]([C:9]2[CH:14]=[CH:13][C:12]([O:15][C:16]([F:19])([F:18])[F:17])=[CH:11][CH:10]=2)[CH:4]=1.[I-:20].[Na+].COC(C)(C)C>CC(C)=O>[I:20][CH2:2][C:3]1[N:7]([CH3:8])[N:6]=[C:5]([C:9]2[CH:14]=[CH:13][C:12]([O:15][C:16]([F:19])([F:18])[F:17])=[CH:11][CH:10]=2)[CH:4]=1

Komponenten

5

Versuchsvorschrift

A suspension of 5-chloromethyl-1-methyl-3-(4-trifluoromethoxy-phenyl)-1H-pyrazole (3.2 g, 11 mmol; example 19 a]) and sodium iodide (8.25 g, 55 mmol) in acetone (56 ml) was heated under reflux conditions for 30 min. Tert butyl methyl ether was added, the solid was filtered off and the filtrate was brought to dryness under reduced pressure. The residue was dissolved in tert butyl methyl ether, washed with ice water/brine 1/1 and the aqueous layer was extracted two times with tert butyl methyl ether. The combined extracts were washed with aqueous sodium thiosulfate solution and brine and dried over sodium sulfate. The solvent was removed under reduced pressure to give the title compound as yellow oil which was used in the next step without further purification.

Aufarbeitung

  1. filtrationthe solid was filtered off
  2. dissolutionThe residue was dissolved in tert butyl methyl ether
  3. washwashed with ice water/brine 1/1
  4. extractionthe aqueous layer was extracted two times with tert butyl methyl ether
  5. washThe combined extracts were washed with aqueous sodium thiosulfate solution and brine
  6. dry with materialdried over sodium sulfate
  7. customThe solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-dcdacbeec97744d7b60bd052640eb04c
Quelldatensatz
uspto-grants-2007_09
Patentnummer
US07265149B2

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