Sodium Sulfate → HCID 59421275, Verbindung

HRID 499237Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 499237
[O-:1]S([O-])(=O)=O.[Na+].[Na+].C1C=C(Cl)C=C(C(OO)=O)C=1.[CH2:19]([O:21][C:22]([C:24]1[C:25]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=2[F:38])=[N:26][C:27]([S:30][CH3:31])=[N:28][CH:29]=1)=[O:23])[CH3:20].C([O-])(O)=O.[Na+]>C(Cl)Cl>[CH2:19]([O:21][C:22]([C:24]1[C:25]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=2[F:38])=[N:26][C:27]([S:30]([CH3:31])=[O:1])=[N:28][CH:29]=1)=[O:23])[CH3:20]

Komponenten

6

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A Na2SO4-dried solution of m-CPBA (10.64 g, ca. 45 mmol) in CH2Cl2 (100 mL) was added drop wise to a cold (−65° C.) solution of 4-(2-fluoro-phenyl)-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester in CH2Cl2 (200 mL) keeping the temperature below −65° C. The yellow suspension was allowed to warm to 0° C. over 1 hour. After 3 hours at 0° C., a saturated aqueous NaHCO3 solution (100 mL) was added to quench the reaction. The organic layer was separated, washed with saturated aqueous NaCl solution, dried over Na2SO4, and concentrated. The product was taken up in CH2Cl2 and washed again with a saturated aqueous NaHCO3 solution to remove traces of m-C(P)BA giving 4-(2-fluoro-phenyl)-2-methanesulfinyl-pyrimidine-5-carboxylic acid ethyl ester (12.86 g, >100%).

Aufarbeitung

  1. customthe temperature below −65° C
  2. customto quench
  3. customthe reaction
  4. customThe organic layer was separated
  5. washwashed with saturated aqueous NaCl solution
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. washwashed again with a saturated aqueous NaHCO3 solution
  9. customto remove traces

Quellen und Nachweise

ORD-Eintrag
ord-b95fafd5b47d40919ff8cfceff46b67b
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07767680B2

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