تفاعل #1747841

ord-8555216920a943dc8f3548059f7cd4eb

معادلة التفاعل

CC(C)OB(OC(C)C)OC(C)C
triisopropyl borate
CCCCCC
hexane
[Li][CH2]CCC
n-butyllithium
Cl
hydrochloric acid
Brc1cccc(-c2cccc3ccccc23)c1
1-(3-bromophenyl) naphthalene
OB(O)c1cccc(-c2cccc3ccccc23)c1
3-(1-naphthyl)phenylboronic acid
المردود 71.9%

المذيبات

ظروف التفاعل

درجة الحرارة
-60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThen, the reaction mixture was stirred for two hours at −60 degrees C
  2. 2
    درجة الحرارةThe reaction solution was further cooled down to −60 degrees C
  3. 3
    درجة الحرارةSubsequently, the reaction mixture was warmed up to room temperature
  4. 4
    workup.STIRRINGstirred for 17 hours
  5. 5
    workup.STIRRINGto be stirred for one hour at room temperature
  6. 6
    أخرىAfter the reaction
  7. 7
    تجفيفAfter organic phase thereof was dried with magnesium sulfate
  8. 8
    workup.DISTILLATIONthe solvent was distilled away under reduced pressure
  9. 9
    أخرىBy recrystallizing the obtained solid by toluene

الإجراء التجريبي

Under an argon gas atmosphere, a mixture of 200.0 g (706.3 mmol) of 1-(3-bromophenyl) naphthalene and 2.1 L of dehydrated THF was cooled down to −60 degrees C., and added with 543 mL (847 mmol) of hexane solution of 1.56M n-butyllithium in drops while being stirred. Then, the reaction mixture was stirred for two hours at −60 degrees C. The reaction solution was further cooled down to −60 degrees C. and added with 398.5 g (2.119 mol) of triisopropyl borate in drops. Subsequently, the reaction mixture was warmed up to room temperature, and stirred for 17 hours. The reaction mixture was further added with solution of hydrochloric acid to be stirred for one hour at room temperature. After the reaction, the reaction mixture was further added with toluene, so that aqueous phase thereof was eliminated. After organic phase thereof was dried with magnesium sulfate, the solvent was distilled away under reduced pressure. By recrystallizing the obtained solid by toluene, 126 g of 3-(1-naphthyl)phenylboronic acid was obtained at an yield of 67%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08029697B2uspto-grants-2011_10