HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 2,3,4,5-tetrafluorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trioctylamine | HCID 14227 | — |
| Reactant | Tetrafluorophthalic anhydride | HCID 69545 | — |
| Product | Methyl 2,3,4,5-tetrafluorobenzoate | HCID 600996 | 92.4% |
Reaction Steps
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%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05523476 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-9c1826eb28e6460088ac926d523c93ce |
| Source note | uspto-grants-1996_06 |