HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 385201Erstellt: 24. Oktober 2026
Methyl Acrylate → Trimethyl cyclohexane-1,2,4-tricarboxylate
https://huagongshe.com/de/reaction/385201
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl Acrylate | HCID 7294 | — |
| Edukt | tert-Butylcatechol | HCID 77643 | — |
| Edukt | Dimethyl muconate, (E,E)- | HCID 5370244 | — |
| Lösungsmittel | Diglyme | HCID 8150 | — |
| Produkt | Trimethyl cyclohexane-1,2,4-tricarboxylate | HCID 12616206 | — |
Reaktionsschritte
In a 75 ml sealed tube, a stirred suspension of trans,trans dimethyl muconate (10.0 g, 58.8 mmol), two equivalents of methyl acrylate (10.6 ml, 117.6 mmol), neutral Al2O3 (300 mg of Aldrich 199974, 3 mass percent), and tert-butyl catechol (25 mg, 0.2 mol percent) in diglyme (20 ml, 2.9 M) is heated to 150° C. for 24 hours. After cooling to room temperature, the reaction mixture is filtered, transferred to a flask, and concentrated (0.5 M). Pd/C catalyst is added (856 mg (0.3 mol percent) of Johnson-Matthey 5 percent Pd/C #6) at room temperature. The flask is equipped with a reflux condenser, flitted gas dispersion tube, and internal T probe. Under N2 flow (190 ml/min) and stirring (190 rpm) the mixture is heated to reflux for 27 hours whereby trimethyl trimellitate (46 percent over 2 steps) is formed. Some trimethyl cyclohexane-1,2,4-tricarboxylate is also produced.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08367858B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-71096e43cec245bda0599f72147afd49 |
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| Quellennotiz | uspto-grants-2013_02 |
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