تفاعل #4560

معادلة التفاعل

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

2,4-pentanedione

benzene

sodium

→

product

المردود 16.0%

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

المردود 16.0%

المذيبات

ether

water

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةwas warmed
2. 2
   درجة الحرارةat reflux for 3 hours
3. 3
   درجة الحرارةThe resulting mixture was warmed
4. 4
   درجة الحرارةat reflux for 2.5 hours
5. 5
   أخرىThe organic layer was separated
6. 6
   تجفيفdried over MgSO4
7. 7
   أخرىevaporated to dryness
8. 8
   أخرىThe residue was purified by prep LC
9. 9
   غسيلeluting with 4:1 hexane
10. 10
    استخلاصextracted with two portions of 1% aqueous NaOH
11. 11
    استخلاصextracted with ether
12. 12
    أخرىThe ether layer was evaporated to dryness
13. 13
    أخرىthe residue again purified by prep LC
14. 14
    غسيلeluting with 85:15 hexane
15. 15
    أخرىThis gave a yellow oil which
16. 16
    أخرىwas thoroughly dried

الإجراء التجريبي

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.

المصدر