Reaktion #51272

Reaktionsgleichung

2-methyl-4-bromo-2-butene

3-methoxythiophenol

sodium hydroxide

→

expected compound

Ausbeute 90.4%

1-methoxy-3-(3-methylbut-2-enylsulphanyl)benzene

Ausbeute 90.4%

Lösungsmittel

acetone

acetone

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturthe mixture is heated
2. 2
   Temperaturat reflux for three hours
3. 3
   workup.ADDITIONis added dropwise
4. 4
   TemperaturReflux
5. 5
   Temperaturis maintained for sixteen hours
6. 6
   Sonstigethe reaction mixture is evaporated to dryness
7. 7
   workup.ADDITIONWater is added
8. 8
   Extraktionextraction
9. 9
   Waschenthe organic phase is washed with water
10. 10
    Trocknendried over magnesium sulphate
11. 11
    Filtrationfiltered
12. 12
    Sonstigethe solvents are evaporated
13. 13
    SonstigeThe residue obtained
14. 14
    workup.DISTILLATIONis distilled under reduced pressure (5×10−2 bar/113° C.)

Vorschrift

50.45 g (360.0 mmol) of 3-methoxythiophenol, 360 ml of acetone and 14.40 g (360.0 mmol) of sodium hydroxide pellets are introduced into a one liter round-bottomed flask under a nitrogen atmosphere and the mixture is heated at reflux for three hours. A solution composed of 53.6 g (360.0 mmol) of 2-methyl-4-bromo-2-butene and of 60 ml of acetone is added dropwise. Reflux is maintained for sixteen hours and the reaction mixture is evaporated to dryness. Water is added, extraction is carried out with ethyl acetate, the organic phase is washed with water and then using a saturated sodium chloride solution, dried over magnesium sulphate and filtered, and the solvents are evaporated. The residue obtained is distilled under reduced pressure (5×10−2 bar/113° C.) to produce 67.81 g (90%) of the expected compound in the form or a pale-yellow oil.

Quelle