Phosphorus oxychloride → 2-Chloro-8-fluoroquinoline

HRID 1019785Notes

Reaction equation

HRID 1019785 reaction equation
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[NH:10][C:9](=O)[CH:8]=[CH:7]2.P(Cl)(Cl)([Cl:15])=O>>[Cl:15][C:9]1[CH:8]=[CH:7][C:6]2[C:11](=[C:2]([F:1])[CH:3]=[CH:4][CH:5]=2)[N:10]=1

Participants

3

Conditions

Temperature
125 °C

Procedure

8-Fluoroquinolin-2(1H)-one (26.0 g, 159 mmol) was slurried with phosphoryl trichloride (163 ml, 1.73 mol, 11 eq) and heated to 125° C. for 2 h. The reaction was cooled to rt and poured onto 1.2 L of ice water with vigorous stirring. When the mixture had cooled to rt, the orange solid was filtered and washed with water and dried under vacuum overnight to afford 27 g of crude material. The crude material was recrystallized from hexanes by dissolving in ˜700 mL of hexanes at reflux and decanting away from residual tar. The hexane solution was cooled to 0° C. and the precipitate 2-chloro-8-fluoroquinoline was filtered. The mother liquor was concentrated in vacuo and recrystallized from hexanes to obtain a second crop of 2-chloro-8-fluoroquinoline (21.3 g, 74% total yield).

Workup

  1. temperatureThe reaction was cooled to rt
  2. temperatureWhen the mixture had cooled to rt
  3. filtrationthe orange solid was filtered
  4. washwashed with water
  5. customdried under vacuum overnight
  6. customto afford 27 g of crude material
  7. customThe crude material was recrystallized from hexanes
  8. dissolutionby dissolving in ˜700 mL of hexanes
  9. temperatureat reflux
  10. customdecanting away from residual tar
  11. temperatureThe hexane solution was cooled to 0° C.
  12. filtrationthe precipitate 2-chloro-8-fluoroquinoline was filtered
  13. concentrationThe mother liquor was concentrated in vacuo
  14. customrecrystallized from hexanes

Sources & evidence

ORD record
ord-dbad5c1eb88444dc994d55b2b853fa42
Source dataset
uspto-grants-2014_05
Patent number
US08716290B2

Reaction notes

Loading…