Реакция #4560

Уравнение реакции

2-(4-(4-bromo-2-fluorophenoxy)phenoxy)propanoyl chloride

2,4-pentanedione

benzene

sodium

→

product

Выход 16.0%

3-Acetyl-5-(4-(4-bromo-2-fluorophenoxy)phenoxy)-2,4-hexanedione

Выход 16.0%

Растворители

ether

water

Условия реакции

Обработка

1. 1
   Температураwas warmed
2. 2
   Температураat reflux for 3 hours
3. 3
   ТемператураThe resulting mixture was warmed
4. 4
   Температураat reflux for 2.5 hours
5. 5
   ДругоеThe organic layer was separated
6. 6
   Сушкаdried over MgSO4
7. 7
   Другоеevaporated to dryness
8. 8
   ДругоеThe residue was purified by prep LC
9. 9
   Промывкаeluting with 4:1 hexane
10. 10
    Экстракцияextracted with two portions of 1% aqueous NaOH
11. 11
    Экстракцияextracted with ether
12. 12
    ДругоеThe ether layer was evaporated to dryness
13. 13
    Другоеthe residue again purified by prep LC
14. 14
    Промывкаeluting with 85:15 hexane
15. 15
    ДругоеThis gave a yellow oil which
16. 16
    Другоеwas thoroughly dried

Методика

A mixture of 1.7 g (17 mmol) of 2,4-pentanedione, 30 ml of benzene and 0.26 g (11.3 mmol) of sodium was warmed at reflux for 3 hours. The reaction mixture was cooled to room temperature and a solution of 10 mmol of 2-(4-(4-bromo-2-fluorophenoxy)phenoxy)propanoyl chloride was added dropwise. The resulting mixture was warmed at reflux for 2.5 hours, stirred at room temperature overnight and poured into water and ether. The organic layer was separated, dried over MgSO4 and evaporated to dryness. The residue was purified by prep LC, eluting with 4:1 hexane:acetone. The product was taken up in ether and extracted with two portions of 1% aqueous NaOH. The combined aqueous layers were made acidic with aqueous HCl and extracted with ether. The ether layer was evaporated to dryness and the residue again purified by prep LC, eluting with 85:15 hexane:acetone. This gave a yellow oil which was thoroughly dried to leave 0.70 g product. Calc for C20H18BrFO5 : C, 54.93, H, 4.15. Found: C, 54.13, H, 4.30.

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