Réaction #2006436
ord-e3240a12305545aa8ba5190fb20db763
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Autreequipped with a water condenser, addition funnel and a nitrogen inlet
- 2TempératureThis solution was cooled in an ice/water bath
- 3Températureheated
- 4Températureto reflux for 30 minutes
- 5TempératureThe reaction mixture was cooled to room temperature
- 6Autrequenched with 125 ml of deionized water
- 7AutreThe organic phase was separated
- 8Extractionthe water phase was extracted with 50 ml ether
- 9LavageThe combined ether solutions were washed with 100 ml brine
- 10Séchagedried over anhydrous magnesium sulfate
- 11AutreThe solvent was removed in a rotary evaporator
- 12Autrethe 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.