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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584858Generated: October 25, 2026

5-Aminosalicylic Acid → 2-Hydroxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl-benzylamino)benzoic acid

https://huagongshe.com/reaction/584858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminosalicylic AcidHCID 4075—
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
SolventDimethylformamideHCID 6228—
Product2-Hydroxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl-benzylamino)benzoic acidHCID 995195564%

Reaction Steps

To a solution of 5-aminosalicylic acid (1.02 g, 6.66 mmole, purchased from Aldrich Chemical Company, USA, A7, 980-9) and triethylamine (1 ml) in dried DMF (80 ml) was added 2,3,5,6-tetrafluoro-4-trifloromethylbenzyl bromide (1.23 g, 7.18 mmole) (Aldrich, 40, 640-6) at room temperature under a nitrogen atmosphere. The reaction mixture was stirred for 2 hr at room temperature and then solvent was removed in vacuo. The reaction mixture was diluted with ethyl acetate and then extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous MgSO4. After evaporation of the solvent, the residue was recrystallized from ether/hexane (1:10) to give 1.60 g (64% yield) of 2-hydroxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethylbenzylamino)benzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927303B2
Source datasetuspto-grants-2005_08
ORD IDord-1fd346ee2ba144769333c7ab07fca1b5
Source noteuspto-grants-2005_08