반응 #58897

ord-473f15d3152d4cb6b61fa8db3a5f3858

반응 방정식

O=Cc1cc(O)cc(O)c1
3,5-dihydroxybenzaldehyde
OB(O)c1ccccc1
phenylboronic acid
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
O=S(=O)(OS(=O)(=O)C(F)(F)F)C(F)(F)F
trifluoromethanesulfonic anhydride
O=Cc1cc(O)cc(-c2ccccc2)c1
5-Hydroxy-biphenyl-3-carbaldehyde

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the temperature below 5° C
  2. 2
    세척After 10 min the mixture was washed with water
  3. 3
    농축the organic phase was concentrated under reduced pressure
  4. 4
    온도The mixture was refluxed for 17 h under Argon
  5. 5
    추출extracted with ethyl acetate
  6. 6
    기타Purification by chromatography

실험 절차

A solution of 3,5-dihydroxybenzaldehyde (14.4 mmol) and pyridine (114 mmol) in methylene chloride (20 ml) was slowly added trifluoromethanesulfonic anhydride (36.2 mmol) keeping the temperature below 5° C. After 10 min the mixture was washed with water and the organic phase was concentrated under reduced pressure. The crude brown crystals (6.4 g—product and pyridine −1:1), phenylboronic acid (13.2 mmol), sodium carbonate (39.6 mmol) and dichlorobis(triphenylphosphine)-palladium (II). (3 mol %) was dissolved in DME (40 ml) and water (20 ml). The mixture was refluxed for 17 h under Argon, cooled to room temperature and extracted with ethyl acetate. Purification by chromatography yielded 5-Hydroxy-biphenyl-3-carbaldehyde

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07423181B2uspto-grants-2008_09