반응 #58896

ord-e9f887c92ce84f78af53796f22ec052b

반응 방정식

O=Cc1ccc(O)cc1O
2,4-dihydroxybenzaldehyde
O=S(=O)(OS(=O)(=O)C(F)(F)F)C(F)(F)F
trifluoromethanesulfonic anhydride
[H-].[Na+]
sodium hydride
Cc1ccccc1B(O)O
ortho-tolylboronic acid
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
c1ccncc1
pyridine
CN(C)CCCl
2-dimethylamino ethylchloride
Cc1ccccc1-c1ccc(C=O)c(OCCN(C)C)c1
3-(2-Dimethylamino-ethoxy)-2′-methyl-biphenyl-4-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
    workup.DISSOLUTIONThe crude black oil (4.6 g) was dissolved in DMF (75 ml)
  7. 7
    온도the mixture was heated at 80° C. for 3 days
  8. 8
    세척The mixture was washed with saturated sodium bicarbonate
  9. 9
    농축concentrated under reduced pressure
  10. 10
    기타purified by chromatography
  11. 11
    세척The resulting yellow oil was washed with hot heptane giving the product as relative pure oil (GC-MS)

실험 절차

A solution of 2,4-dihydroxybenzaldehyde (27 mmol) in methylene chloride (10 ml) and pyridine (30 mmol) was slowly added trifluoromethanesulfonic anhydride (32 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 oil (5 g), ortho-tolylboronic acid (20.4 mmol), sodium carbonate (55.5 mmol) and dichlorobis(triphenylphosphine)-palladium (II) (3 mol %) was dissolved in DME (50 ml) and water (20 ml). The mixture was refluxed for 17 h under Argon, cooled to room temperature and extracted with ethyl acetate. The crude black oil (4.6 g) was dissolved in DMF (75 ml) and sodium hydride (60% in oil, 22.5 mmol) was slowly added. A solution of 2-dimethylamino ethylchloride (22.5 mmol) in toluene (120 ml) was added and the mixture was heated at 80° C. for 3 days. The mixture was washed with saturated sodium bicarbonate, concentrated under reduced pressure and purified by chromatography. The resulting yellow oil was washed with hot heptane giving the product as relative pure oil (GC-MS). 1H-NMR (DMSO-d6) δ 10.41 (s, 1H), 7.74 (d, 2H), 7.66-7.55 (m, 1H), 7.36-6.79 (m, 4H), 4.27 (t, 2H), 2.70 (t, 2H), 2.27 (s, 3H), 2.23 (s, 6H).

출처

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