HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 915611Erstellt: 25. Oktober 2026
Diflunisal → 2',4'-Difluoro-4-hydroxy-5-iodo-1,1'-biphenyl-3-carboxylic acid
https://huagongshe.com/reaction/915611
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diflunisal | HCID 3059 | — |
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Sodium Pyrosulfite | HCID 656671 | — |
| Edukt | Thallium(1+);2,2,2-trifluoroacetate | HCID 21902506 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2',4'-Difluoro-4-hydroxy-5-iodo-1,1'-biphenyl-3-carboxylic acid | HCID 4369563 | — |
Reaktionsschritte
A mixture of 20.6 g of thallium trifluoroacetate (TTFA, 31.9 mmol) and trifluoroacetic acid (TFA, 50 ml) was stirred in a flask until the TTFA dissolved. This solution was added at room temperature to a flask containing 51 g (205 mmol) of diflunisal and it was stirred for 30 min. A solution of potassium iodide (KI, 40.9 g, 245.6 mmol) in 120 ml of water was slowly added to the mixture. After the reaction finished, the product was worked up. First, sodium metabisulphite (NaS2O5, 5.01 g, 26.4 mmol) was added to reduce the species of TI (III) to TI (I), and then a solution of sodium hydroxide was added to neutralize the TFA. It was extracted with dichloromethane and the organic phase was washed with water and dried over magnesium sulphate. The solvent was evaporated at low pressure and a crude was obtained of 96% purity, which was purified by chromatography on a silica gel column using the appropriate eluents.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07265245B2 |
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| Quelldatensatz | uspto-grants-2007_09 |
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| ORD ID | ord-10b9ed656e3b40069c8a6f6652458f9c |
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| Quellennotiz | uspto-grants-2007_09 |
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