Ethanol → Ethyl chloronicotinate

To a mixture of 2-hydroxynicotinic acid (13.91 g., 0.1 mole) and phosphorus pentachloride (42 g., 0.2 mole) was added phosphorus oxychloride (25 ml., excess) and then stirred at room temperature for 30 minutes. This was then heated at 120° C. for 2 hours. The reaction mixture was then concentrated in vacuo until a red viscous mass was obtained. The latter was cooled in an ice water bath and 45 ml. absolute ethanol was added first slowly and then rapidly. It was then refluxed for 30 min. and cooled. Most of the excess ethanol was removed under vacuo and the remaining mass was diluted with water (90 ml.). The aqueous solution was neutralized with 10% sodium carbonate solution and then extracted with 2×100 ml. portions of dichloromethane. The organic layer was washed with 2N NaOH solution followed by water and brine. It was dried and then concentrated to give a pale yellow liquid which was purified by distillation under reduced pressure (20 mm. Hg, b.p. 140°-44° C.) to give ethyl 2-chloronicotinate in 60-65% yield. A fore-run at 80°-110° C. (5-10%) was discarded which consisted mainly of ethyl 2-ethoxynicotinate.

1. temperatureThis was then heated at 120° C. for 2 hours
2. concentrationThe reaction mixture was then concentrated in vacuo until a red viscous mass
3. customwas obtained
4. temperatureThe latter was cooled in an ice water bath
5. temperatureIt was then refluxed for 30 min.
6. temperaturecooled
7. customMost of the excess ethanol was removed under vacuo
8. additionthe remaining mass was diluted with water (90 ml.)
9. extractionextracted with 2×100 ml
10. washThe organic layer was washed with 2N NaOH solution
11. customIt was dried
12. concentrationconcentrated
13. customto give a pale yellow liquid which
14. distillationwas purified by distillation under reduced pressure (20 mm. Hg, b.p. 140°-44° C.)

ORD record

ord-d0ca2bb5fa8e4a7e9c2ffd5aff410073

Source dataset

uspto-grants-1993_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05248781