Реакция #51272

Уравнение реакции

2-methyl-4-bromo-2-butene

3-methoxythiophenol

sodium hydroxide

→

expected compound

Выход 90.4%

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

Выход 90.4%

Растворители

acetone

acetone

Условия реакции

Обработка

1. 1
   Температураthe mixture is heated
2. 2
   Температураat reflux for three hours
3. 3
   workup.ADDITIONis added dropwise
4. 4
   ТемператураReflux
5. 5
   Температураis maintained for sixteen hours
6. 6
   Другоеthe reaction mixture is evaporated to dryness
7. 7
   workup.ADDITIONWater is added
8. 8
   Экстракцияextraction
9. 9
   Промывкаthe organic phase is washed with water
10. 10
    Сушкаdried over magnesium sulphate
11. 11
    Фильтрацияfiltered
12. 12
    Другоеthe solvents are evaporated
13. 13
    ДругоеThe residue obtained
14. 14
    workup.DISTILLATIONis distilled under reduced pressure (5×10−2 bar/113° C.)

Методика

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.

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