反应详情

A stirred solution of diisopropylamine (14 mL) in dry tetrahydrofuran (150 mL), is treated dropwise with a solution of butyl lithium in hexanes (40 mL; 2.5 M), under nitrogen, while keeping the temperature at below −70° C. The resulting mixture is then stirred for a further period of 30 minutes at below −70° C. The stirred mixture, while it is still maintained at below −70° C., is then treated dropwise with a solution of 4-picoline (9.3 g) in dry tetrahydrofuran (20 mL). The stirred mixture is maintained at below −70° C. for a further 45 minutes. The stirred mixture, while it is still maintained at below −70° C., is then treated with a solution of 3-cyclopentyloxy-4-methoxybenzaldehyde (22.0 g) in dry tetrahydrofuran (100 mL), and it is stirred at below −70° C. for a further 30 minutes. The resulting mixture is then allowed to warm to room temperature overnight, and then treated with saturated aqueous ammonium chloride solution (200 mL). The layers are separated and the aqueous layer is further extracted with ethyl acetate (3×300 mL). The combined organic extracts are dried over magnesium sulfate and evaporated to dryness. The resulting residue is recrystallized from ethyl acetate, to give (±)-1-(3-cyclopentyloxy-4-methoxyphenyl)-2-(pyrid-4-yl)ethanol (28.5 g), in the form of a cream solid, m.p. 102-103° C.

1. customat below −70° C
2. temperatureThe stirred mixture, while it is still maintained at below −70° C.
3. temperatureThe stirred mixture is maintained at below −70° C. for a further 45 minutes
4. temperatureThe stirred mixture, while it is still maintained at below −70° C.
5. stirringis stirred at below −70° C. for a further 30 minutes
6. customThe layers are separated
7. extractionthe aqueous layer is further extracted with ethyl acetate (3×300 mL)
8. dry with materialThe combined organic extracts are dried over magnesium sulfate
9. customevaporated to dryness
10. customThe resulting residue is recrystallized from ethyl acetate