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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259962Generated: October 25, 2026

Trioctylamine → 2,4,5-Trifluoro-3-methoxybenzoic acid

https://huagongshe.com/reaction/259962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrioctylamineHCID 14227—
ReactantSodium HydroxideHCID 14798—
Reactant1,2-Benzenedicarboxylic acid, 3,4,6-trifluoro-5-methoxy-HCID 10198851—
Product2,4,5-Trifluoro-3-methoxybenzoic acidHCID 273397087%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523476
Source datasetuspto-grants-1996_06
ORD IDord-36462188366f496bb120dc6cdbae06e1
Source noteuspto-grants-1996_06