反应详情

Sodium borohydride (2.40 g, 63.4 mmol)) was added to the 4,4′-bis(3-formyl-carbazol-9-yl)biphenyl (2) (3.42 g, 6.33 mmol) in THF (1.2 L) and the resulting suspension was stirred at room temperature for 24 h. Once the reaction was complete, the mixture was slowly poured into water (400 ml) and the mixture was left to stir at room temperature for a further 30 min. The reaction mixture was acidified to pH 6 with hydrochloric acid (5M) and the product was extracted with dichloromethane (3×300 ml). The combined organic phase was washed with water (400 ml) and brine (400 ml), dried (MgSO4), filtered and the filtrate evaporated to dryness. The crude product was purified by chromatography on silica using 50% THF/toluene as the eluent The product, 4,4′-bis(3-(hydroxymethyl)carbazol-9-yl)(3) was obtained as a pale yellow solid (3.22 g, 94%) with m.p. 268° C. (dec). 1H n.m.r.: (300 MHz, CDCl3): δ 8.23 (2H, d, J 7.61 Hz, aromatic H); 8.18 (2H, s, aromatic H); 8.06 (4H, d, J 8.19 Hz, aromatic H); 7.75 (4H, J 8.19 Hz, aromatic H); 7.50-7.38 (8H, m, aromatic H), 7.29 (2H, m, aromatic H); 5.25 (2H, t, J 5.58 Hz, OH); 4.68 (4H, d, J 5.56 Hz, CH2). λmax(CH2Cl2): 216 nm (ε/Lmol−1 cm−1 177 455), 240 (57 873), 271 (56 595), 294 (55 330) 329 (37 758). FTIR (solid): 3343, 1604, 1500, 1485, 1455, 1362, 1330, 1230, 803, 745 cm−1. m/z (TOF) 544 (M+).

1. waitthe mixture was left
2. stirringto stir at room temperature for a further 30 min
3. extractionthe product was extracted with dichloromethane (3×300 ml)
4. washThe combined organic phase was washed with water (400 ml) and brine (400 ml)
5. dry with materialdried (MgSO4)
6. filtrationfiltered
7. customthe filtrate evaporated to dryness
8. customThe crude product was purified by chromatography on silica using 50% THF/toluene as the eluent The product