HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 517327Erstellt: 25. Oktober 2026
Formic Acid → 5-Ethoxycarbonylfuran-2-ylacetic acid
https://huagongshe.com/reaction/517327
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formic Acid | HCID 284 | — |
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Ethyl 5-(chloromethyl)-2-furancarboxylate | HCID 263166 | — |
| Katalysator | Rhodium, di-mu-chlorobis((1,2,5,6-eta)-1,5-cyclooctadiene)di- | HCID 6436379 | — |
| Produkt | 5-Ethoxycarbonylfuran-2-ylacetic acid | HCID 69842632 | — |
Reaktionsschritte
5-Chloromethyl-2-furancarboxylic acid ethyl ester (1.0 g, 5.3 mmol), potassium iodide (0.044 g, 0.27 mmol), and chloro(1,5-cyclooctadiene)rhodium(I) dimer (0.26 g, 0.53 mmol) were dissolved in formic acid (25 mL), and the mixture was stirred at 75° C. for 6 hours under a carbon monoxide atmosphere. The solvent was evaporated, and the residue was partitioned between ethyl acetate and aqueous sodium hydrogen carbonate solution. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The drying agent was filtered off, the solvent was evaporated, and the residue was purified by silica gel column chromatography to give the title compound (0.61 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09115107B2 |
|---|
| Quelldatensatz | uspto-grants-2015_08 |
|---|
| ORD ID | ord-d4044127998548c698cb29c9f07ac67e |
|---|
| Quellennotiz | uspto-grants-2015_08 |
|---|