P-Cresol → Benzene, 1-(2,2-dimethylpropoxy)-4-methyl-

HRID 911447Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 911447
[CH:1]1[C:6]([OH:7])=[CH:5][CH:4]=[C:3]([CH3:8])[CH:2]=1.N(C(OC(C)C)=O)=NC(OC(C)C)=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:42](O)[C:43]([CH3:46])([CH3:45])[CH3:44]>C1COCC1>[CH3:42][C:43]([CH3:46])([CH3:45])[CH2:44][O:7][C:6]1[CH:5]=[CH:4][C:3]([CH3:8])=[CH:2][CH:1]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of p-cresol (526 mg, 4.87 mmol) in THF (50 mL), add with stirring diisopropyl azodicarboxylate (2.16 mL, 10.7 mmol) followed by triphenylphosphine (306 mg, 11.7 mmol) and neopentyl alcohol (5.15 g, 58.4 mmol). Heat at 60° C. for 3 h, cool to ambient temperature and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc to give the desired intermediate as a colorless oil.

Aufarbeitung

  1. temperaturecool to ambient temperature
  2. concentrationconcentrate in vacuo
  3. customPurify by chromatography on silica gel eluting with hexane/EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-8fc367222dc347828e622b9ce3e701ec
Quelldatensatz
uspto-grants-2011_09
Patentnummer
US08022062B2

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