Methanol → 4-Ethylresorcinol

HRID 1072948Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1072948
[CH3:1][C:2]([C:4]1[CH:5]=[CH:6][C:7]([OH:11])=[CH:8][C:9]=1[OH:10])=O.CO.[H][H]>[Ni].[Pd].C(O)(=O)C>[CH2:2]([C:4]1[CH:5]=[CH:6][C:7]([OH:11])=[CH:8][C:9]=1[OH:10])[CH3:1]

Komponenten

7

Reaktionsbedingungen

Temperatur
72.5 °C

Versuchsvorschrift

2,4-Dihydroxy acetophenone (76 g, 0.5 mole) was charged in a 1 liter autoclave reactor along with methanol (300 ml), acetic acid (5 ml), and Raney Nickel (15.2 g washed several times with water and water/methanol) and 750 mg of Pd/C. The pH of the system was 5.0. The autoclave was checked for leaks with nitrogen. The autoclave was pressurized to 500 psi with hydrogen and stirred at 70-75° C. up to 8 hrs. During this time 97% of the theoretical value for hydrogen was consumed. The reaction was vented and the contents were filtered through a milipore filter to give a yellow solution. Concentration of this solution in vacuo gave a solid. This solid was crystalized from 1,2-dichloroethane to give 4-ethyl resorcinol in 85% isolated yield. The unreacted 2,4-dihydroxy acetophenone was recovered (−13%) from the reaction mixture and was recycled. The structure of 4-ethyl resorcinol and 2,4-dihydroxy acetophenone were characterized by NMR (see FIG. 1), Gas Chromatography (see FIG. 2), IR (See FIG. 3) and Mass spectroscopy. The mass spectroscopy indicated that the mass was 138.

Aufarbeitung

  1. customDuring this time 97% of the theoretical value for hydrogen was consumed
  2. filtrationthe contents were filtered through a milipore
  3. filtrationfilter
  4. customto give a yellow solution
  5. customConcentration of this solution in vacuo gave a solid
  6. customThis solid was crystalized from 1,2-dichloroethane

Quellen und Nachweise

ORD-Eintrag
ord-0785870683a348adabc3f32bf6bacb96
Quelldatensatz
uspto-grants-2005_06
Patentnummer
US06911562B2

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