Hydrochloric Acid → 6-Chloro-3-methylquinoline

Temperature

100 °C

To a solution of 4-chloroaniline (9.59 g, 75.2 mmol) in dioxane (112 mL) was added a 6 M aqueous solution of HCl (180 mL). The reaction mixture was heated to 100° C. and a solution of 2-methyl-2-propene-1,1-diol acetate (15.5 g, 90.3 mmol) in dioxane (20 mL) was added dropwise during 1 h under an argon atmosphere. The reaction mixture was stirred for 2 h at 120° C. after which an aliquot was taken and analyzed by HPLC. Since some starting material was still left, the reaction mixture was cooled down to 100° C. and another portion of 2-methyl-2-propene-1,1-diol actetate (5.2 g, 30 mmol) was added during 1 h. After heating for 2 h at 120° C., the reaction mixture was cooled down again to 100° C. and a final portion of 2-methyl-2-propene-1,1-diol actetate (5.2 g, 30 mmol) was added during 1 h at 100° C. Heating was continued for 30 min. at 120° C. After cooling to ambient temperature the reaction mixture was diluted with water (100 mL) and extracted with 2-methoxy-2-methylpropane (2×200 mL). The combined organic phases were extracted with a 4 M HCl solution (100 mL). The combined aqueous phases were basified to pH 9 with a 4 M NaOH solution and extracted with TBME (3×200 mL). The combined organic layers were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated at reduced pressure to afford a brown oil. The crude product was purified by flash column chromatography (silica gel, cyclohexane/EtOAc 95:5) to afford 6-chloro-3-methylquinoline as a pale brown crystalline solid (6.32 g, 35.6 mmol, 47%). 1H NMR (400 MHz, CDCl3, 298 K): δ=8.78 (d, J=2.2 Hz, 1H), 8.03 (d, J=8.8 Hz, 1H), 7.86 (bs, 1H), 7.75 (d, J=2.2 Hz, 1H), 7.60 (dd, J=8.8 Hz, 2.2 Hz, 1H), 2.55 (s, 3H). MS (ES+): 178 (M(C10H835ClN)+H)+.

1. waitSince some starting material was still left
2. temperaturethe reaction mixture was cooled down to 100° C.
3. temperatureAfter heating for 2 h at 120° C.
4. temperaturethe reaction mixture was cooled down again to 100° C.
5. temperatureHeating
6. waitwas continued for 30 min. at 120° C
7. temperatureAfter cooling to ambient temperature the reaction mixture
8. extractionextracted with 2-methoxy-2-methylpropane (2×200 mL)
9. extractionThe combined organic phases were extracted with a 4 M HCl solution (100 mL)
10. extractionextracted with TBME (3×200 mL)
11. washThe combined organic layers were washed with brine (100 mL)
12. dry with materialdried over Na2SO4
13. filtrationfiltered
14. concentrationconcentrated at reduced pressure
15. customto afford a brown oil
16. customThe crude product was purified by flash column chromatography (silica gel, cyclohexane/EtOAc 95:5)

ORD record

ord-6fc5f1865e4741aa8424cf972d65d79b

Source dataset

uspto-grants-2010_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07781438B2