Dimethylformamide → 2-Fluoro-4,6-dihydroxybenzaldehyde

HRID 1955160Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1955160
CN(C)[CH:3]=[O:4].P(Cl)(Cl)(Cl)=O.[OH:11][C:12]1[CH:13]=[C:14]([F:19])[CH:15]=[C:16]([OH:18])[CH:17]=1>O>[OH:11][C:12]1[CH:17]=[C:16]([OH:18])[CH:15]=[C:14]([F:19])[C:13]=1[CH:3]=[O:4]

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 126587785-Fluororesorcinol

Produkt 1

HCID 220104032-Fluoro-4,6-dihydroxybenzaldehydeAusbeute 27,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Dimethylformamide (12.7 g) was added to vigorously stirred phosphorous oxychloride (14.4 g) at 0° C. The reaction mixture was stirred at this temperature for 30 minutes, then 3,5-dihydroxyfluorobenzene (6 g) was added. The sticky red syrup was allowed to warm to room temperature and stirred for 2 hours, then left to stand for 14 hours. Water (100 ml) was added and the mixture extracted three times with ethyl acetate (100 ml). The combined organic extracts were washed with brine (100 ml), dried over magnesium sulphate and evaporated. The residue was purified by flash chromatography on silica eluting with a mixture of ethyl acetate and pentane (1:2, v/v). Fractions homogeneous in the required product were combined and evaporated to give an orange solid which was triturated with ethyl acetate to give the title compound (2 g) as a yellow solid.

Aufarbeitung

  1. stirringstirred for 2 hours
  2. waitleft
  3. waitto stand for 14 hours
  4. extractionthe mixture extracted three times with ethyl acetate (100 ml)
  5. washThe combined organic extracts were washed with brine (100 ml)
  6. dry with materialdried over magnesium sulphate
  7. customevaporated
  8. customThe residue was purified by flash chromatography on silica eluting with a mixture of ethyl acetate and pentane (1:2
  9. customevaporated
  10. customto give an orange solid which
  11. customwas triturated with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-af430eeaa17b423d951ef05cdbf58312
Quelldatensatz
uspto-grants-2000_09
Patentnummer
US06124343

Notizen zur Reaktion

Wird geladen…