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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktThiazolidinedioneHCID 5437—
EduktPiperidineHCID 8082—
Edukt4-[3-(1-Adamantyl)-4,5-methylenedioxyphenyl]-benzaldehydeHCID 10155443—
LösungsmittelAcetic AcidHCID 176—
Produkt4-[3-(1-Adamantyl)-4,5-methylenedioxyphenyl]-benzylidene-2,4-thiazolidinedioneHCID 7241655376,5%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07153875B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-03d80f3777614300a7ea32710f1653ea
Quellennotizuspto-grants-2006_12