反应详情

温度

-70 °C

To a stirred solution of N,N,N′-trimethylethylenediamine (1.9 mL, 15 mmol) in anhydrous THF (65 mL) under argon at −70° C. was slowly added 1.6M n-BuLi in hexanes (9.0 mL, 14 mmol). After stirring at −70° C. for 15 minutes, 6-methoxy-nicotinaldehyde (1.3 g, 9.8 mmol) was added dropwise. After the addition was complete, stirring was continued at −70° C. for another 15 minutes. Then 1.6M n-BuLi in hexanes (10 mL, 16 mmol) was added dropwise and stirring continued at −45° C. for 4 h. The solution was cooled to −70° C. and then a solution of iodine (3.0 g, 12 mmol) and anhydrous THF (25 mL) was added dropwise. When the addition was complete, stirring was continued at −70° C. for 30 minutes and then at RT for 3 h. The crude product was taken up in ether (40 mL) and washed successively with saturated ammonium chloride (2×40 mL) and 5% sodium thiosulfate (2×20 mL). The organic phase was dried, filtered and concentrated. Purification by column chromatography with EtOAc-heptanes (1:1) as eluent gave 0.41 g (15% yield) of 4-iodo-6-methoxynicotinaldehyde.

1. customat −70° C.
2. additionAfter the addition
3. stirringstirring
4. waitwas continued at −70° C. for another 15 minutes
5. stirringstirring
6. waitcontinued at −45° C. for 4 h
7. temperatureThe solution was cooled to −70° C.
8. additionWhen the addition
9. stirringstirring
10. waitwas continued at −70° C. for 30 minutes
11. waitat RT for 3 h
12. washwashed successively with saturated ammonium chloride (2×40 mL) and 5% sodium thiosulfate (2×20 mL)
13. customThe organic phase was dried
14. filtrationfiltered
15. concentrationconcentrated
16. customPurification by column chromatography with EtOAc-heptanes (1:1) as eluent