反应详情

温度

0 °C

Isoquinoline-3-carbonitrile (1.76 g, 11.4 mmole) is dissolved in 10 ml tetrahydrofuran in an oven dried 100 ml two neck round bottom flask under nitrogen. The solution is cooled to 0° C., is diluted with 5 ml diethyl ether, and is treated with methyl magnesium bromide in ether (5.7 ml, 17.1 mmole). The reaction is warmed to reflux for one hour, is cooled to 0° C., and is quenched with 15 ml 6 M hydrochloric acid. The reaction mixture is warmed to 50° C. for one hour, is cooled, and is poured into 75 ml 2N sodium hydroxide. The mixture is extracted with 3×50 ml ethyl acetate and the combined organics are dried over potassium carbonate. The dried organics are concentrated in vacuo to a crude orange solid. The crude material is chromatographed over 60 g silica gel (230-400 mesh), eluting with 20% acetone/hexane, while collecting 22 ml fractions. Fractions 7-11 are combined and concentrated to provide 1.7 g (87%) of 3-acetyl-isoquinoline.

1. dry with materialdried 100 ml two neck round bottom flask under nitrogen
2. additionis diluted with 5 ml diethyl ether
3. temperatureThe reaction is warmed
4. temperatureto reflux for one hour
5. temperatureis cooled to 0° C.
6. customis quenched with 15 ml 6 M hydrochloric acid
7. temperatureThe reaction mixture is warmed to 50° C. for one hour
8. temperatureis cooled
9. additionis poured into 75 ml 2N sodium hydroxide
10. extractionThe mixture is extracted with 3×50 ml ethyl acetate
11. dry with materialthe combined organics are dried over potassium carbonate
12. concentrationThe dried organics are concentrated in vacuo to a crude orange solid
13. customThe crude material is chromatographed over 60 g silica gel (230-400 mesh)
14. washeluting with 20% acetone/hexane
15. customwhile collecting 22 ml fractions
16. concentrationconcentrated