HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2051533Erstellt: 25. Oktober 2026
Hydroquinone → 4-Methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione
https://huagongshe.com/reaction/2051533
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydroquinone | HCID 785 | — |
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | 1,3-Pentadiene | HCID 62204 | — |
| Edukt | 1,3-Pentadiene, (3Z)- | HCID 643785 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4-Methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione | HCID 12726603 | 99% |
Reaktionsschritte
Maleic anhydride (68.6 parts) and 70 parts of toluene were introduced into a pressure autoclave, and melted at 55° C. Then, 0.162 part of hydroquinone was added, and 130.9 parts (corresponding to 1.1 moles of trans-1,3-pentadiene per mole of maleic anhydride) of crude trans-1,3-pentadiene composed of 40 % of trans-1,3-pentadiene, 20 % of cis-1,3-pentadiene and 40 % of pentanes was continuously added over 6 hours at 50° C. The temperature was then raised to 60° C., and the reaction was carried out for 3 hours. After the reaction, the reaction mixture was distilled at 90° C. under atmospheric pressure to remove volatile components to give 3-methyltetrahydrophthalic anhydride (melting point 61° C.) in a yield of 99 % as a Diels-Alder reaction product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05019599 |
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| Quelldatensatz | uspto-grants-1991_05 |
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| ORD ID | ord-61db99f76e62470e820b5e99396eddbf |
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| Quellennotiz | uspto-grants-1991_05 |
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