تفاعل #2487420

ord-a5ff2a8054dc49f794f3cf9ceb627d96

معادلة التفاعل

Brc1ccc(Br)c2ccccc12
1,4-dibromonaphthalene
[Li][CH2]CCC
n-butyllithium
C[Si](C)(C)Cl
chlorotrimethylsilane
CCO
EtOH
C[Si](C)(C)c1ccc(Br)c2ccccc12
(4-bromonaphth-1-yl)trimethylsilane

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONare subsequently slowly added at this temperature
  2. 2
    workup.ADDITIONis added to the solution
  3. 3
    أخرىobtained in this way
  4. 4
    درجة الحرارةthe mixture is slowly warmed to room temperature
  5. 5
    أخرىthe organic phase is separated off
  6. 6
    تجفيفdried over magnesium sulfate
  7. 7
    أخرىevaporated
  8. 8
    أخرىThe oil obtained in this way
  9. 9
    workup.DISTILLATIONis distilled at 115-135° C.
  10. 10
    أخرى1.7 mbar, giving 80 g (286 mmol) (corresponding to 88% of theory) of the product

الإجراء التجريبي

A solution of 114.38 g (400 mmol) of 1,4-dibromonaphthalene and 1 l of THF (absolute) is cooled to −78° C. under protective gas, 160 ml (400 mmol) of n-butyllithium (2.5M in n-hexane) are subsequently slowly added at this temperature, and the mixture is stirred at −78° C. for a further 30 h. A mixture of 52.3 ml (400 mmol) of chlorotrimethylsilane in 200 ml of THF (absolute) is added to the solution obtained in this way, and the mixture is slowly warmed to room temperature. After addition of 150 ml of EtOH and subsequently 300 ml of water, the organic phase is separated off, dried over magnesium sulfate and evaporated. The oil obtained in this way is distilled at 115-135° C. and 1.7 mbar, giving 80 g (286 mmol) (corresponding to 88% of theory) of the product having a purity of greater than 99.0% according to HPLC.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08795847B2uspto-grants-2014_08