تفاعل #65906

معادلة التفاعل

1,3-di-t-butylbenzene

bromine

→

title compound

المردود 99.9%

2,4-bis(1,1-dimethylethyl)-1-bromobenzene

المردود 99.9%

المذيبات

acetic acid

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONAfter the addition
2. 2
   workup.STIRRINGthe reaction mixture was stirred for a further 45 minutes
3. 3
   درجة الحرارةAfter cooling
4. 4
   ترشيحthe precipitated silver bromide was filtered off
5. 5
   غسيلwashed with acetic acid
6. 6
   أخرىThe combined filtrates were partitioned between dichloromethane and water
7. 7
   استخلاصthe aqueous layer was further extracted with dichloromethane
8. 8
   غسيلThe combined organic extracts were washed with aqueous sodium bisulfite
9. 9
   تجفيفdried over sodium sulfate
10. 10
    ترشيحfiltered
11. 11
    أخرىevaporated
12. 12
    أخرىAcetic acid was then removed by azeotropic distillation with heptane
13. 13
    workup.DISTILLATIONDistillation of the residue under reduced pressure

الإجراء التجريبي

To a solution of 5.00 g (26.3 mmoles) of 1,3-di-t-butylbenzene in 15 ml of acetic acid was added 4.47 g (26.3 mmoles) of silver nitrate. The mixture was stirred in an oil bath at 75°-80° and then bromine (4.21 g, 26.3 mmoles) was added in small portions over 2 hours. After the addition was complete, the reaction mixture was stirred for a further 45 minutes. After cooling, the precipitated silver bromide was filtered off and washed with acetic acid. The combined filtrates were partitioned between dichloromethane and water and the aqueous layer was further extracted with dichloromethane. The combined organic extracts were washed with aqueous sodium bisulfite, dried over sodium sulfate, filtered, and evaporated. Acetic acid was then removed by azeotropic distillation with heptane. Distillation of the residue under reduced pressure gave 7.07 g of the title compound, b.p. 82°-84° C. (1 mm). The structural assignment was supported by 1H NMR and 13C NMR.

المصدر