반응 #469308

ord-d9054bf4db814d3b9bdeae44438c20d9

반응 방정식

CC(C)OB(OC(C)C)OC(C)C
triisopropylborate
Brc1ccc(-c2ccccc2)cc1
4-bromobiphenyl
[Li][CH2]CCC
n-butyllithium
OB(O)c1ccc(-c2ccccc2)cc1
4-Biphenylboronic acid

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITAfter 10 minutes
  2. 2
    기타partitioned between EtOAc (50 mL) and 10% aqueous HCl (50 mL)
  3. 3
    기타The aqueous layer was separated
  4. 4
    추출extracted with more EtOAc
  5. 5
    세척The combined organic layers were washed with brine
  6. 6
    건조dried over Na2SO4
  7. 7
    농축concentrated
  8. 8
    기타to give a crude product which

실험 절차

4-Biphenylboronic acid was prepared differently than described in the literature (see Yabroff, D. L.; Branch, G. E.; Bettman, B. J. Am. Chem. Soc. 1934, 56, 1850-1857). To a solution of 4-bromobiphenyl (2.00 g, 8.58 mmol) in THF (20 mL) at −78° C. was added n-butyllithium (4.0 mL of 2.5 M in hexanes) in a slow stream via syringe. After 15 minutes, triisopropylborate (3.0 mL, 13 mmol) was added in a slow stream via syringe. After 10 minutes, the resultant homogeneous solution was allowed to warm to ambient temperature over 45 minutes and partitioned between EtOAc (50 mL) and 10% aqueous HCl (50 mL). The aqueous layer was separated and extracted with more EtOAc. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated to give a crude product which was triturated with hexanes to yield 1.53 g (90%) of 4-biphenylboronic acid as a white solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06306892B1uspto-grants-2001_10