Réaction #2146734
ord-380fb7015ad04bac9aa279c4a61dcb75
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1Températurethe reaction mixture was subsequently heated
- 2Températureto reflux for 3 h
- 3TempératureAfter the reaction mixture had cooled to room temp.
- 4Autrethe ethanol was removed in a rotary evaporator under reduced pressure
- 5workup.ADDITIONthe resulting residue diluted with 300 mL of water
- 6ExtractionThe crude product was extracted twice with 500 mL of ether each, and the combined organic extracts
- 7Lavagewere washed twice with 300 mL of brine
- 8SéchageAfter drying with sodium sulphate and removal of the solvent under reduced pressure
- 9Autrethe resulting residue (51.2 g) was purified by flash chromatography (1.00 kg of silica gel, pentane/ether, 9:1, Rf=0.11)
Mode opératoire
In the next step, 55.0 g (278 mmol) of this (5Z)-3-methylnon-5-enyl acetate was dissolved in 600 mL of a 1:1 mixture of ethanol and water. With vigorous stirring, 55.5 g (1.39 mol) of sodium hydroxide was added, and the reaction mixture was subsequently heated to reflux for 3 h. After the reaction mixture had cooled to room temp., the ethanol was removed in a rotary evaporator under reduced pressure, and the resulting residue diluted with 300 mL of water. The crude product was extracted twice with 500 mL of ether each, and the combined organic extracts were washed twice with 300 mL of brine. After drying with sodium sulphate and removal of the solvent under reduced pressure, the resulting residue (51.2 g) was purified by flash chromatography (1.00 kg of silica gel, pentane/ether, 9:1, Rf=0.11) to provide 39.9 g (92%) of (5Z)-3-methylnon-5-en-1-ol as a colourless liquid.