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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 458258Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/458258

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Aminosalicylic AcidHCID 4075—
EduktTriethylamineHCID 8471—
Edukt4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromideHCID 127137—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Hydroxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl-benzylamino)benzoic acidHCID 995195564%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07189878B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-d7c8a53bf59f4d8ea62f5a479429024f
Quellennotizuspto-grants-2007_03