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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 5-Aminosalicylic Acid | HCID 4075 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide | HCID 127137 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-Hydroxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl-benzylamino)benzoic acid | HCID 9951955 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07189878B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-d7c8a53bf59f4d8ea62f5a479429024f |
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| Quellennotiz | uspto-grants-2007_03 |
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