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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270789Generated: November 3, 2026

2-((tert-Butoxycarbonyl)amino)-5-(trifluoromethoxy)benzoic acid → 2-amino-5-(trifluoromethoxy)benzoic Acid

https://huagongshe.com/reaction/1270789

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((tert-Butoxycarbonyl)amino)-5-(trifluoromethoxy)benzoic acidHCID 2773441—
Solvent1,4-DioxaneHCID 31275—
Product2-amino-5-(trifluoromethoxy)benzoic AcidHCID 11085349—

Reaction Conditions

Temperature80 °C

Reaction Steps

The above benzoic acid (120 g, 0.37 mol) is suspended in 1,4-dioxane (200 mL), stirred and warmed to 80° C. until dissolved. The solution is allowed to cool to room temperature and hydrogen chloride is bubbled into the reaction mixture for 30 minutes. Stirring is continued for 2 hours, during which time a precipitate forms. The precipitate is collected and washed with ice-cold water (1000 mL) and Et2O (500 mL) to give 5-trifluoromethoxyanthranilic acid as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202364B2
Source datasetuspto-grants-2007_04
ORD IDord-794df99dcc324112aff9a421c2cb406e
Source noteuspto-grants-2007_04