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Phosphorus oxychloride → 4-Allyloxy-2,6-dimethyl-benzaldehyde

HRID 618516
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 618516
CN([CH:9]=[O:10])C1C=CC=CC=1.P(Cl)(Cl)(Cl)=O.[CH3:16][C:17]1[CH:18]=[C:19]([O:24][CH2:25][CH:26]=[CH2:27])[CH:20]=[C:21]([CH3:23])[CH:22]=1>>[CH2:25]([O:24][C:19]1[CH:20]=[C:21]([CH3:23])[C:22]([CH:9]=[O:10])=[C:17]([CH3:16])[CH:18]=1)[CH:26]=[CH2:27]
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Komponenten

4

Edukt 3

HCID 24813Phosphorus oxychlorideHCID 66737N-MethylformanilideHCID 257959Allyl 3,5-dimethylphenyl ether

Produkt 1

HCID 185158104-Allyloxy-2,6-dimethyl-benzaldehydeAusbeute 51 %

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

N-methyl formanilide, 20.5 ml (166 mmole), was chilled to 13°, where it began to solidify. Phosphorus oxychloride, 14.4 ml (155 mmole), was added with stirring, under nitrogen. After 25 minutes, the temperature was 45°. 3,5-Dimethyl-allyloxy benzene, 16.2 g (100 mmole), prepared as describe above, was added with stirring and heated in a 70° C. oil bath. The reaction exothermed to 93° C. and was stirred under nitrogen for 30 minutes. The bath was removed and when the temperature reached 35°, the product was dissolved in chloroform. Ice was added, the layers were separated and washed once with water, twice with sodium bicarbonate, once with water and once with brine. The product was chromatographed down 500 ml of silica, eluting with chloroform to give 9.67 g (51%) of subtitled product which was used without further purification.

Aufarbeitung

  1. customwas 45°
  2. additionwas added
  3. stirringwith stirring
  4. customexothermed to 93° C.
  5. stirringwas stirred under nitrogen for 30 minutes
  6. customThe bath was removed
  7. customreached 35°
  8. dissolutionthe product was dissolved in chloroform
  9. additionIce was added
  10. customthe layers were separated
  11. washwashed once with water, twice with sodium bicarbonate, once with water and once with brine
  12. customThe product was chromatographed down 500 ml of silica
  13. washeluting with chloroform

Quellen und Nachweise

ORD-Eintrag
ord-d9d06ead6bf34d35873feab82f6a1d41
Quelldatensatz
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05952360

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