Reaction #347140
ord-9c1826eb28e6460088ac926d523c93ce
Reaction equation
tetrafluorophthalic anhydride
tri-n-octylamine
methanol
→
3,4,5,6-tetrafluorobenzoic acid methyl ester
Yield 92.4%
Reagents
None
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1OtherInto a 100 ml glass reactor equipped with a reflux condenser and a stirrer
- 2OtherThen, the mixture was reacted at 140° C. for 4 hours
- 3OtherAfter completion of the reaction
- 4Otherthe reaction mixture was separated by distillation
Procedure
Into a 100 ml glass reactor equipped with a reflux condenser and a stirrer, 20 g (0.091 mol) of the tetrafluorophthalic anhydride prepared in Example 3 and 32.2 g (0.091 mol) of tri-n-octylamine were charged and 3.5 g (0.109 mol) of methanol was dropwise added thereto. Then, the mixture was reacted at 140° C. for 4 hours. After completion of the reaction, the reaction mixture was separated by distillation to obtain 17.5 g of 3,4,5,6-tetrafluorobenzoic acid methyl ester. The yield was 92.3%.