Réaction #2006436

ord-e3240a12305545aa8ba5190fb20db763

Équation de réaction

CCC1(O)CCCCC1OC
1-ethyl-2-methoxycyclohexanol
[Li][CH2]CCC
n-butyllithium
CCCCCC
hexane
C=C(C)C(=O)Cl
methacryloyl chloride
C=C(C)C(=O)OC1(CC)CCCCC1OC
1-ethyl-2-methoxycyclohexyl methacrylate

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreequipped with a water condenser, addition funnel and a nitrogen inlet
  2. 2
    TempératureThis solution was cooled in an ice/water bath
  3. 3
    Températureheated
  4. 4
    Températureto reflux for 30 minutes
  5. 5
    TempératureThe reaction mixture was cooled to room temperature
  6. 6
    Autrequenched with 125 ml of deionized water
  7. 7
    AutreThe organic phase was separated
  8. 8
    Extractionthe water phase was extracted with 50 ml ether
  9. 9
    LavageThe combined ether solutions were washed with 100 ml brine
  10. 10
    Séchagedried over anhydrous magnesium sulfate
  11. 11
    AutreThe solvent was removed in a rotary evaporator
  12. 12
    Autrethe crude product was chromatographed on a neutral alumina column

Mode opératoire

1-ethyl-2-methoxycyclohexanol from the previous step (10 g, 0.063 mole) in 50 ml ether was placed in a three neck flask equipped with a water condenser, addition funnel and a nitrogen inlet. This solution was cooled in an ice/water bath and n-butyllithium, 1.6 molar in hexane (45 ml, 0.072 mole) was added dropwise. The contents were allowed to warm to room temperature and stirred for 30 minutes. The mixture was cooled again in ice/water bath and methacryloyl chloride (7.31 g, 0.070 mole) in 25 ml ether was added dropwise and heated to reflux for 30 minutes. The reaction mixture was cooled to room temperature and quenched with 125 ml of deionized water. The organic phase was separated and the water phase was extracted with 50 ml ether. The combined ether solutions were washed with 100 ml brine and dried over anhydrous magnesium sulfate. The solvent was removed in a rotary evaporator and the crude product was chromatographed on a neutral alumina column using hexane as elutant. The product was a clear liquid (9.79 g) which was characterized by NMR and IR.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08168366B2uspto-grants-2012_05