反应详情

At ambient temperature, to a stirred solution containing 2-n-butylbenzofuran-3-carboxaldehyde (0.888 g, 4.77 mmol) and 4-aminophenol hydrochloride in MeOH (7 mL) was added sodium cyanoborohydride (0.330 g, 5.25 mmol). After 24 h, the reaction was carefully quenched with 3N HCl, diluted with H2O and extracted with CH2Cl2. The organic extracts were washed with sat. aq. NaHCO3, dried and concentrated. Purification on silica gel eluting with a 20 & 40% EtOAc/pet. ether step gradient gave the title compound as a pale yellow solid. 1H NMR (CDCl3) δ 0.93 (t, 3 H), 1.38 (sextet, 2 H), 1.70 (quintet, 2 H), 2.79 (t, 2 H), 4.27 (s, 1 H), 4.35 (br. s, 1 H), 6.62 (d, 2 H), 6.75 (d, 2 H), 7.18-7.26 (m, 3 H), 7.41 (d, 1 H), 7.54 (d, 1 H).

1. customthe reaction was carefully quenched with 3N HCl
2. additiondiluted with H2O
3. extractionextracted with CH2Cl2
4. washThe organic extracts were washed with sat. aq. NaHCO3
5. customdried
6. concentrationconcentrated
7. customPurification on silica gel eluting with a 20 & 40% EtOAc/pet. ether step gradient