HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Carbon Dioxide → 2,5-Thiophenedicarboxylic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 2,5-Diiodothiophene | HCID 69368 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2,5-Thiophenedicarboxylic acid | HCID 20273 | 60% |
Reaktionsschritte
To a solution of 2.5 g. of 2,5-diiodothiophene in 5 ml. of anhydrous tetrahydrofuran and 5 ml. of anhydrous ether at -5°, under nitrogen, is added dropwise over the period of one-half hour 14.92 ml. of 1.5 M n-butyllithium. After standing for two hours at 0°, carbon dioxide gas is added to the mixture for one-half hour at 0° and one-half hour at 10°. The reaction mixture is stirred at room temperature overnight. Water is added, the aqueous layer is acidified with 2N sulfuric acid, and the solution is then extracted with ether, the combined organic phases are washed with water and brine, dried over calcium sulfate, filtered and the solvent removed to yield 2,5-thiophenedicarboxylic acid (about 60% pure).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04093622 |
| Quelldatensatz | uspto-grants-1978_06 |
| ORD ID | ord-9d0ebfaef5924de18cd24edb2b897718 |
| Quellennotiz | uspto-grants-1978_06 |