反应详情

3-piperidin-1-yl-propan-1-ol (3.66 g, 25.6 mmol), 4-nitrophenol (2.96 g, 21.3 mmol) and triphenylphosphine (6.71 g, 25.6 mmol) were dissolved in dry tetrahydrofuran in a current of nitrogen, and cooled on the ice bath. Diisopropyl azodicarboxylate (5.0 mL, 25.6 mmol) was dripped in, and stirred at room temperature for 40 hours. The reaction liquid was concentrated, diethyl ether was added, and the solid precipitate was filtered off. The filtrate was concentrated, the product purified by silica gel column chromatography (chloroform/methanol=100/0-95/5), and the target substance (3.49 g, 62%) was thus obtained as a light yellow oily residue.

1. customThe reaction liquid
2. concentrationwas concentrated
3. additiondiethyl ether was added
4. filtrationthe solid precipitate was filtered off
5. concentrationThe filtrate was concentrated
6. customthe product purified by silica gel column chromatography (chloroform/methanol=100/0-95/5)
7. customthe target substance (3.49 g, 62%) was thus obtained as a light yellow oily residue