Reaktion #52567

ord-60a582a1f67047778e5b4ab65a829ff1

Reaktionsgleichung

O=[N+]([O-])c1ccc(O)cc1
4-nitrophenol
Cl
HCl
COCOC
formaldehyde dimethylacetal
O=[N+]([O-])c1ccc(O)c(CCl)c1
2-chloromethyl-4-nitrophenol
Ausbeute 76.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA 5-necked flask equipped with mechanical overhead stirrer, gas inlet tube
  2. 2
    Temperaturreflux condenser
  3. 3
    SonstigeGaseous HCl was bubbled through the mixture for 4 hours
  4. 4
    SonstigeDuring this time a thick white precipitate formed
  5. 5
    TemperaturThe suspension was cooled to 0° C.
  6. 6
    Sonstigethe precipitate was isolated by vacuum filtration
  7. 7
    Sonstigethe yellow powder was dried over night under vacuum

Vorschrift

A 5-necked flask equipped with mechanical overhead stirrer, gas inlet tube, reflux condenser and a thermometer was charged with 4-nitrophenol (100 g, 0.72 mol). Concentrated HCl 932%, 1.3 L), conc. H2SO4 (98%, 10 mL) and formaldehyde dimethylacetal (152.4 g, 2 moles) were added and the mixture was heated to 70° C. Gaseous HCl was bubbled through the mixture for 4 hours. During this time a thick white precipitate formed. The suspension was cooled to 0° C., the precipitate was isolated by vacuum filtration and the yellow powder was dried over night under vacuum to give 108.76 g of slightly impure 2-chloromethyl-4-nitrophenol (about 76% yield).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06855833B2uspto-grants-2005_02