2-Bromoaniline → 8-Bromo-2-methylquinoline

Temperatur

0 °C

To a refluxed solution of 2-bromoaniline (5.0 g, 29.1 mmol) in 6 N hydrochloric acid (15 mL) was added crotonaldehyde (2.2409 g, 32.0 mmol) drop wise. After heated under reflux for 8 h, the reaction mixture was cooled down and washed with 20 ml of ether, followed by addition of zinc chloride (3.95 g). The reaction mixture was stirred for 30 min at room temperature and another 15 min at 0° C. to give yellow solid. The solid was collected and washed with 3 N cold hydrochloric acid, and then suspended in 2-propanol (20 mL) and stirred for 5 min at room temperature. The solid was filtered and washed with 2-propanol until the washing becomes colorless, then washed with 20 mL of ether and dried with air. The solid was suspended in 15 mL of cold water and 5 mL of concentrated ammonium hydroxide was added. Shake it and then extract with 3×20 mL of ether. Dried over magnesium sulfate and concentrated to give a dark solid. Purification by chromatography (EtOAC/Hexanes 10:90) yielded a white solid product. (3.62 g, 56%) 1H NMR(400 MHz CDCl3) δ8.02 (2H, t, J=8.4 Hz), 7.73 (1H, d, J=8 Hz), 7.33 (2H, t, J=8), 2.82 (3H, s); 13C NMR (300 MHz CDCl3) δ160.2, 144.7, 136.4, 132.8, 127.6, 127.3, 125.9, 124.0, 122.7, 25.6; EIMS, m/z 221/223 (M/(M+2)); Anal. Calcd for C10H8BrN: C, 54.08; H, 3.63; N, 6.31. Found: C, 54.25; H, 3.41; N, 5.89.

1. temperatureAfter heated
2. temperatureunder reflux for 8 h
3. temperaturethe reaction mixture was cooled down
4. washwashed with 20 ml of ether
5. additionfollowed by addition of zinc chloride (3.95 g)
6. customto give yellow solid
7. customThe solid was collected
8. washwashed with 3 N cold hydrochloric acid
9. stirringstirred for 5 min at room temperature
10. filtrationThe solid was filtered
11. washwashed with 2-propanol until the washing
12. washwashed with 20 mL of ether
13. customdried with air
14. addition5 mL of concentrated ammonium hydroxide was added
15. extractionShake it and then extract with 3×20 mL of ether
16. dry with materialDried over magnesium sulfate
17. concentrationconcentrated
18. customto give a dark solid
19. customPurification by chromatography (EtOAC/Hexanes 10:90)
20. customyielded a white solid product

ORD-Eintrag

ord-7cc3ac4b407b46908d135dcde55df93b

Quelldatensatz

uspto-grants-2010_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07767817B2