Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 371139Erstellt: 24. Oktober 2026

1,3-Cyclohexadiene → 3a-(3,4-dichlorophenyl)-2-ethyl-3a,4,7,7a-tetrahydro-4,7-ethano-1H-isoindol-1,3(2H)-dione

https://huagongshe.com/de/reaction/371139

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-CyclohexadieneHCID 11605—
Edukt3-(3,4-dichlorophenyl)-1-ethyl-1H-pyrrole-2,5-dioneHCID 13519573—
KatalysatorMethylene blue cationHCID 4139—
LösungsmittelDichloromethaneHCID 6344—
Produkt3a-(3,4-dichlorophenyl)-2-ethyl-3a,4,7,7a-tetrahydro-4,7-ethano-1H-isoindol-1,3(2H)-dioneHCID 1351956657,4%

Reaktionsschritte

A solution of 7.5 g of the above maleimide, 2.25 g of 1,3-cyclohexadiene, and 10 mg of methylene blue in 25 ml of dichloromethane was heated at reflux for 5 hours, then an additional one ml of the diene was added and the solution was heated for 24 hours. The cooled reaction mixture was subjected to high pressure liquid chromatography on a silica gel column eluting with hexane:ethyl acetate (4:1) and gave 5.58 g of 3a-(3,4-dichlorophenyl)-2-ethyl-3a,4,7,7a-tetrahydro-4,7-ethano-1H-isoindol-1,3(2H)-dione as a white solid, mp 122°-126° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04529736
Quelldatensatzuspto-grants-1985_07
ORD IDord-6c8109afb7414cbd97405ce1beacba2f
Quellennotizuspto-grants-1985_07