반응 #1747843

ord-30f615f0cda0480cbd50100b9d6ce7a3

반응 방정식

CC(C)OB(OC(C)C)OC(C)C
triisopropyl borate
CCCCCC
hexane
[Li][CH2]CCC
n-butyllithium
Cl
hydrochloric acid
Brc1ccc(-c2cccc3ccccc23)cc1
1-(4-bromophenyl) naphthalene
OB(O)c1ccc(-c2cccc3ccccc23)cc1
4-(1-naphthyl)phenylboronic acid
수율 68.9%

반응 조건

온도
-60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThen, the reaction mixture was stirred for two hours at −60 degree C
  2. 2
    workup.STIRRINGSubsequently, the reaction mixture was stirred for 17 hours at room temperature
  3. 3
    workup.STIRRINGto be stirred for one hour at room temperature
  4. 4
    기타After the reaction
  5. 5
    건조After organic phase thereof was dried with magnesium sulfate
  6. 6
    workup.DISTILLATIONthe solvent was distilled away under reduced pressure
  7. 7
    기타By recrystallizing the obtained solid by toluene

실험 절차

Under an argon gas atmosphere, a mixture of 208.8 g (737.4 mmol) of 1-(4-bromophenyl) naphthalene and 2.1 L of dehydrated THF was cooled down to −60 degrees C., and added with 567 mL (884.9 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 degree C. 416 g (2.21 mol) of triisopropyl borate was dropped into the reaction solution at −60 degrees C. Subsequently, the reaction mixture was stirred for 17 hours at room temperature. 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 4-(1-naphthyl)phenylboronic acid was obtained at an yield of 67%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08029697B2uspto-grants-2011_10