HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2424853Erstellt: 26. Oktober 2026
Sodium Carbonate → 5-[4-(5-Formylfuran-2-yl)-phenyl]-furan-2-carboxaldehyde
https://huagongshe.com/reaction/2424853
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 1,4-Benzenediboronic acid | HCID 230478 | — |
| Edukt | 5-Bromofuran-2-carbaldehyde | HCID 600328 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 5-[4-(5-Formylfuran-2-yl)-phenyl]-furan-2-carboxaldehyde | HCID 23160969 | 93% |
Reaktionsschritte
To a stirred solution of 5-bromofuran-2-carboxaldehyde (10 mmol), and tetrakis(triphenylphosphine)palladium (400 mg) in toluene (20 mL) under a nitrogen atmosphere was added 10 mL of a 2 M aqueous solution of Na2CO3 followed by 1,4-phenylenebisboronic acid (5 mmol) in 6 mL of methanol. The vigorously stirred mixture was warmed to 80° C. for 12 h. The solvent was evaporated, the precipitate was partitioned between methylene chloride (300 mL) and 2 M aqueous Na2CO3 (15 mL) containing 5 mL of concentrated ammonia. The organic layer was dried (Na2SO4), and then concentrated to dryness under reduced pressure to afford 11 in 93% yield; mp 233-234° C. (EtOH). 1H NMR (DMSO-d6); δ 9.64 (s, 2H), 8.01 (s, 4H), 7.70 (d, J=3.6 Hz, 2H), 7.43 (d, J=3.6 Hz, 2H). MS (ESI) m/e (rel. int.): 266 (M+, 100), 238 (5), 209 (25). Anal. Calc. for C16H10O4: C %, 72.16; H %, 3.78; Found. C %, 72.41; H %, 3.93.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07964619B2 |
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| Quelldatensatz | uspto-grants-2011_06 |
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| ORD ID | ord-2f875aed50934d09bfd5dc94de2468e2 |
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| Quellennotiz | uspto-grants-2011_06 |
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