Reaction #1884995

ord-6ae797dfaf714ea596086c22c9298f6b

Reaction equation

O=Cc1ccc(F)c(F)c1
3,4-di-fluoro-benzaldehyde
O=C(O)CC(=O)O
malonic acid
C1CCNCC1
piperidine
c1ccncc1
pyridine
Cl
HCl
O=C(O)C=Cc1ccc(F)c(F)c1
3,4-di-fluoro-cinnamic acid
Yield 95.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureAfter heating it to 80° C.
  2. 2
    workup.STIRRINGthe mixture was stirred for 12 hours
  3. 3
    OtherAfter the reaction
  4. 4
    Temperaturethe resulting solution cooled down to room temperature
  5. 5
    FiltrationThe resulting powder was filtered
  6. 6
    Washwashed with water
  7. 7
    Otherdried in a vacuum oven

Procedure

10 g (70.4 mmol) of 3,4-di-fluoro-benzaldehyde, 14.65 g (2 eq.) of malonic acid, and 0.59 g (0.1 eq.) of piperidine were added to 16.7 g (3 eq.) of pyridine and stirred at room temperature for about 1 hour. After heating it to 80° C., the mixture was stirred for 12 hours. After the reaction, the resulting solution cooled down to room temperature and was slowly added with 1M HCl until it was titrated to about pH 4. The resulting powder was filtered and washed with water, and then dried in a vacuum oven. (Yield: 95%)

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08343597B2uspto-grants-2013_01