반응 #1747837

ord-7950353d11f84a3498874d087b7569fc

반응 방정식

CC(C)OB(OC(C)C)OC(C)C
triisopropyl borate
CCCCCC
hexane
[Li][CH2]CCC
n-butyllithium
Cl
hydrochloric acid
Brc1cccc(-c2ccc3ccccc3c2)c1
2-(3-bromophenyl) naphthalene
OB(O)c1cccc(-c2ccc3ccccc3c2)c1
3-(2-naphthyl)phenylboronic acid
수율 67.9%

반응 조건

온도
-10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThen, the reaction mixture was stirred for one hour at 0 degrees C
  2. 2
    온도The reaction solution was further cooled down to −78 degrees C
  3. 3
    workup.STIRRINGSubsequently, the reaction mixture was stirred for 17 hours at room temperature
  4. 4
    workup.STIRRINGto be stirred for one hour at room temperature
  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 212 g (748 mmol) of 2-(3-bromophenyl) naphthalene and 3 L of dehydrated THF was cooled down to −10 degrees C., and added with 600 mL (948 mmol) of hexane solution of 1.6M n-butyllithium in drops while being stirred. Then, the reaction mixture was stirred for one hour at 0 degrees C. The reaction solution was further cooled down to −78 degrees C. and added with 450 g (2.39 mol) of triisopropyl borate in drops. 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. The reaction mixture was further added with 3 L of 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-(2-naphthyl)phenylboronic acid was obtained at an yield of 67%.

출처

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