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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroquinoneHCID 785—
EduktMaleic AnhydrideHCID 7923—
Edukt1,3-PentadieneHCID 62204—
Edukt1,3-Pentadiene, (3Z)-HCID 643785—
LösungsmittelTolueneHCID 1140—
Produkt4-Methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dioneHCID 1272660399%

Reaktionsbedingungen

Temperatur60 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05019599
Quelldatensatzuspto-grants-1991_05
ORD IDord-61db99f76e62470e820b5e99396eddbf
Quellennotizuspto-grants-1991_05