반응 #488331

ord-da7dcdebc0d744e9bee3b252288ecd1b

반응 방정식

Cc1cccc(CC(=O)c2ccccc2)c1
N-methoxy-N-methyl-2-phenyl-acetamide
Cc1cccc(CC(=O)c2ccccc2)c1
1-phenyl-2-m-tolylethanone
Cc1cccc(CC(=O)c2ccccc2)c1
Intermediate 4
Cc1cccc(CC(=O)c2ccccc2)c1
1-phenyl-2-m-tolylethanone
Brc1ccc(-c2ccccc2)cc1
4-bromobiphenyl
[Li][CH2]CCC
n-BuLi
O=C(Cc1ccccc1)c1ccc(-c2ccccc2)cc1
1-(biphenyl-4-yl)-2-phenylethanone
수율 24.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe mixture was stirred at −78° C. for 2 h
  2. 2
    기타The reaction was quenched with saturated NH4Cl aqueous solution
  3. 3
    추출extracted with EtOAc
  4. 4
    건조The organic layer was dried over Na2SO4
  5. 5
    농축concentrated in vacuo
  6. 6
    기타purified by column chromatography (PE:EtOAc=20:1)

실험 절차

To a solution of 4-bromobiphenyl (683 mg, 2.9 mmol) in anhydrous THF (5 mL) was added n-BuLi (1.2 mL, 2.9 mmol) dropwise at −78° C. After being stirred at the temperature for 0.5 h, a solution of N-methoxy-N-methyl-2-phenyl-acetamide (prepared following step 1 of Intermediate 4) (500 mg, 2.8 mmol) in anhydrous THF (5 mL) was added via a syringe, and the mixture was stirred at −78° C. for 2 h. The reaction was quenched with saturated NH4Cl aqueous solution, and extracted with EtOAc. The organic layer was dried over Na2SO4, concentrated in vacuo, and purified by column chromatography (PE:EtOAc=20:1) to give 1-(biphenyl-4-yl)-2-phenylethanone (180 mg, yield 24%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08741915B2uspto-grants-2014_06