HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 860523Erstellt: 25. Oktober 2026
Toluene → 4-[3-(1-Adamantyl)-4,5-methylenedioxyphenyl]-benzylidene-2,4-thiazolidinedione
https://huagongshe.com/reaction/860523
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Thiazolidinedione | HCID 5437 | — |
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | 4-[3-(1-Adamantyl)-4,5-methylenedioxyphenyl]-benzaldehyde | HCID 10155443 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 4-[3-(1-Adamantyl)-4,5-methylenedioxyphenyl]-benzylidene-2,4-thiazolidinedione | HCID 72416553 | 76,5% |
Reaktionsschritte
A solution of toluene (10 mL), piperidine (10 μL), acetic acid (10 μL), 4-[3-(1-adamantyl)-4,5-methylenedioxyphenyl]-benzaldehyde (0.400 g, 1.11 mmol) and 2,4-thiazolidinedione (0.130 g, 1.11 mmol) was heated at reflux overnight under an argon atmosphere. The reaction mixture was cooled to room temperature, and the resulting crystalline compound was filtered, washed with toluene and ethanol. The yellow solid was dried under high vacuum to afford 0.390 g (76%) of 4-[3-(1-adamantyl)-4,5-methylenedioxyphenyl]-benzylidene-2,4-thiazolidinedione, mp 308° (dec). 1H NMR (500 MHz; DMSO-d6): 1.74 (s, 6H), 2.04 (s, 9H), 6.05 (s, 2H), 7.06 (d, J=1.5 Hz, 1H), 7.20 (d, J=1.5 Hz, 1H), 7.63 (d, J=8.0 Hz, 2H), 7.78 (d, J=8.0 Hz, 2H), 7.81 (s, 1H), 12.5–12.7 (brs, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07153875B2 |
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| Quelldatensatz | uspto-grants-2006_12 |
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| ORD ID | ord-03d80f3777614300a7ea32710f1653ea |
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| Quellennotiz | uspto-grants-2006_12 |
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