반응 #58896
ord-e9f887c92ce84f78af53796f22ec052b
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후처리
- 1기타the temperature below 5° C
- 2세척After 10 min the mixture was washed with water
- 3농축the organic phase was concentrated under reduced pressure
- 4온도The mixture was refluxed for 17 h under Argon
- 5추출extracted with ethyl acetate
- 6workup.DISSOLUTIONThe crude black oil (4.6 g) was dissolved in DMF (75 ml)
- 7온도the mixture was heated at 80° C. for 3 days
- 8세척The mixture was washed with saturated sodium bicarbonate
- 9농축concentrated under reduced pressure
- 10기타purified by chromatography
- 11세척The 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).