تفاعل #362823

معادلة التفاعل

ammonium chloride

1-bromo-3,5-difluorobenzene

magnesium

3,5-difluorophenyltrimethyltin

boron trichloride

trimethyltin chloride

→

Dichloro-3,5-difluorophenylborane

المردود 81.0%

المذيبات

ethyl ether

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةAfter the reaction mixture was refluxed for 2 hrs
2. 2
   درجة الحرارةkept refluxing for one more hour
3. 3
   أخرىThe organic layer of 3,5-difluorophenyltrimethyltin was separated
4. 4
   workup.DISTILLATIONpurified by distillation in a 62% yield

الإجراء التجريبي

1-bromo-3,5-difluorobenzene (38.6 g, 0.2 mol) was added slowly to a mixture of magnesium turnings (4.8 g, 0.2 mol) in 200 ml anhydrous ethyl ether. After the reaction mixture was refluxed for 2 hrs, trimethyltin chloride (40 g, 0.2 mol) was dropped in to the solution and kept refluxing for one more hour. Then the reaction mixture was hydrolyzed by saturated ammonium chloride. The organic layer of 3,5-difluorophenyltrimethyltin was separated and purified by distillation in a 62% yield. Then the 3,5-difluorophenyltrimethyltin (11 g, 0.04 mol) was reacted with boron trichloride (11 g, 0.093 mol) in a sealed tube at 0° C. for 1 hr and at room temperature for 12 hrs. Dichloro-3,5-difluorophenylborane (6.3 g, 0.032 mol) was obtained from the reaction in 81% yield. Dichloro-3,5-difluorophenylborane (5.84 g, 0.03 mol) was added into a solution containing perfluoropinacol (10 g, 0.03 mol) in 50 ml anhydrous chloroform at −40° C. Then the reaction mixture was stirred continuously at room temperature for 4 hrs. Then the insoluble material was filtered off from the solution. The chloroform solvent was removed by evaporation. The pure product compound 4 (10 g, 0.022 mol) was obtained by distillation of the residue in 73% yield. Boiling point: 80° C./14 mm-Hg. NMR (CDCl3 ppm) δ: 6.9-7.4 (m, 1H), 7.35-7.7 (m, 2H). IR (neat cm−1), ν 3092.0, 1593.8, 1480.6, 1432.0, 1388.2, 1248.9, 1109.8, 1080.5, 986.9, 952.8, 889.6, 870.4, 748.2, 721.8.

المصدر