Reaction #1519074

ord-6e4271858e7d42cfa2f6e9b2657c0378

Reaction equation

Cl
HCl
CN(C)C=O
dimethylformamide
COc1c(F)cccc1Cl
2-chloro-6-fluoroanisole
[Li][CH2]CCC
n-BuLi
COc1c(Cl)ccc(C=O)c1F
light gold oil
Yield 75.0%
COc1c(Cl)ccc(C=O)c1F
4-chloro-2-fluoro-3-methoxybenzaldehyde
Yield 75.0%

Conditions

Temperature
-49°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONDuring the addition the reaction
  2. 2
    workup.ADDITIONafter addition
  3. 3
    workup.ADDITIONwas added
  4. 4
    Otherthe temperature below −50° C
  5. 5
    TemperatureThe reaction was warmed to room temperature
  6. 6
    workup.WAITwas continued for 2 hours
  7. 7
    OtherThe phases were separated
  8. 8
    Concentrationthe organic phase concentrated
  9. 9
    WashThe solution was washed twice with 500 mL of aqueous 10% HCl
  10. 10
    DryingThe organic phase was dried over MgSO4
  11. 11
    Filtrationfiltered
  12. 12
    Concentrationconcentrated to 372 g of a light gold oil (93% pure by GC)
  13. 13
    workup.DISTILLATIONThis oil was distilled bulb to bulb

Procedure

To a solution of 2-chloro-6-fluoroanisole (321.2 g) in 2 L of dry tetrahydrofuran (THF), cooled to −70° C., was added 890 mL of 2.5 M n-BuLi in hexane over 30 min with good mechanical stirring. During the addition the reaction warmed to −48 to −50° C. and was held there for 15 min after addition was complete. The solution was cooled to −75° C. before a solution of 177 g of dimethylformamide (DMF) in 100 mL of THF was added keeping the temperature below −50° C. The reaction was warmed to room temperature and 260 g of 37% aqueous HCl was slowly added and stirring was continued for 2 hours. The phases were separated and the organic phase concentrated and taken into 2 L of ether. The solution was washed twice with 500 mL of aqueous 10% HCl. The organic phase was dried over MgSO4, filtered and concentrated to 372 g of a light gold oil (93% pure by GC). This oil was distilled bulb to bulb to give 282 g (75% yield) of a light gold oil that solidified upon standing. A small sample was crystallized from pentane to give fine white needles; MP 44-45° C.; 1H NMR (CDCl3, 300 MHz) δ 10.3 (s, 1H); 7.5 (dd, 1H, J=6.6, 8.5 Hz); 7.3 (m, 1H); 4.0 (s, 3H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07611647B2uspto-grants-2009_11