تفاعل #81602

معادلة التفاعل

hydrogen

Sodium hydride

1,3,5-tribromobenzene

4-fluorophenol

→

title compound

المردود 32.5%

1,3-Dibromo-5-(4-fluorophenoxy)benzene

المردود 32.5%

المذيبات

collidine

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةwas heated
2. 2
   درجة الحرارةunder reflux
3. 3
   درجة الحرارةIt was then cooled
4. 4
   ترشيحfiltered
5. 5
   غسيلThe residue was washed with ethyl acetate
6. 6
   أخرىthe combined filtrate and washings were partitioned between ethyl acetate and water
7. 7
   غسيلThe organic layer was washed twice with brine
8. 8
   أخرىevaporated
9. 9
   workup.DISSOLUTIONThe residue was dissolved in ethyl acetate
10. 10
    ترشيحthe solution was filtered
11. 11
    غسيلwashed several times with citric acid solution
12. 12
    تجفيفdried (MgSO4)
13. 13
    أخرىThe solvent was evaporated
14. 14
    workup.DISSOLUTIONthe residue was dissolved in hot hexane
15. 15
    ترشيحThe solution was filtered
16. 16
    أخرىthe filtrate was evaporated
17. 17
    أخرىThe residue was chromatographed on silica

الإجراء التجريبي

Sodium hydride (3.24 g of 60% suspension in mineral oil was added portionwise to a stirred mixture of 1,3,5-tribromobenzene (76.4 g), 4-fluorophenol (18.16 g), and cuprous oxide (11.6 g) in collidine (400 ml) at room temperature. When evolution of hydrogen had ceased the mixture was heated under reflux with stirring for 8 hours. It was then cooled and filtered. The residue was washed with ethyl acetate followed by concentrated aqueous ammonia, and the combined filtrate and washings were partitioned between ethyl acetate and water. The organic layer was washed twice with brine and evaporated. The residue was dissolved in ethyl acetate, and the solution was filtered, washed several times with citric acid solution and dried (MgSO4). The solvent was evaporated, and the residue was dissolved in hot hexane. The solution was filtered and the filtrate was evaporated. The residue was chromatographed on silica using hexane as eluent to give the title compound as an oil (18.21 g), Rf 0.31(SS 2). Found: C,41.71; H,1.97. C12H7Br2FO requires C,41.66; H,2.04%.

المصدر