HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trioctylamine → 2,4,5-Trifluoro-3-methoxybenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trioctylamine | HCID 14227 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,2-Benzenedicarboxylic acid, 3,4,6-trifluoro-5-methoxy- | HCID 10198851 | — |
| Product | 2,4,5-Trifluoro-3-methoxybenzoic acid | HCID 2733970 | 87% |
Reaction Steps
Into a 100 ml three necked flask, 10 g (0.04 mol) of the 4-methoxy-3,5,6-trifluorophthalic acid prepared in Example 22 and 14.2 g (0.04 mol) of trioctylamine were charged, and the mixture was reacted at 140° C. for 4 hours with stirring. After completion of the reaction, 30 ml of a 20% sodium hydroxide aqueous solution was added thereto and stirred. The aqueous phase was separated and neutralized with a 10% hydrochloric acid aqueous solution and extracted with ethyl acetate. Then, the solvent was distilled off to obtain 7.17 g of 3-methoxy-2,4,5-triflourobenzoic acid. The yield was 87.0%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05523476 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-36462188366f496bb120dc6cdbae06e1 |
| Source note | uspto-grants-1996_06 |