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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252359Generated: October 26, 2026

Ethylene → 7-Ethenylbicyclo[4.2.0]octa-1,3,5-triene

https://huagongshe.com/reaction/1252359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyleneHCID 6325—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-Bromobicyclo[4.2.0]octa-1,3,5-trieneHCID 11789868—
Reactant2-Ethenylbicyclo[4.2.0]octa-1,3,5-trieneHCID 71341282—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product7-Ethenylbicyclo[4.2.0]octa-1,3,5-trieneHCID 2753007—
Product2-Ethenylbicyclo[4.2.0]octa-1,3,5-trieneHCID 71341282—

Reaction Conditions

Temperature125 °C

Reaction Steps

The monomer is prepared by heating a mixture of 4-bromobenzocyclobutene with 4-vinylbenzocyclobutene at reflux. Vinylbenzocyclobutene is prepared by adding 0.98 g of 4-bromobenzocyclobutene, 0.04 g palladium (II) acetate, and 0.17 g of tri-o-tolylphosphine to a mixture of 100 ml acetonitrile and 0.6 g of triethylamine in a 450 ml Parr pressure reactor. The reactor is pressurized with 250 psig ethylene. The mixture is heated to 125° C. and stirred for 16 hours. The apparatus is cooled and the remaining ethylene is vented. The product is washed with water and 5 percent hydrochloric acid and dried over MgSO4. The solvent is removed to provide 4-vinylbenzocyclobutene. A 2.4 g sample of 4-bromobenzocyclobutene, a 1.7 g of 4-vinylbenzocyclobutene, a 2.4 g of tri-n-butylamine, a 100 mg of tri-o-tolylphosphine, 29 mg palladium (II) acetate and 10 ml acetonitrile are added to a fask equipped with a reflux condenser, nitrogen inlet, and magnetic stirrer. The reaction mixture is heated to reflux under nitrogen for 4 hours. The solution is cooled to room temperature and stirred into 60 ml of 10 percent hydrochloric acid solution. The precipitate is collected by filtration, washed with water and air dried. The product is recrystallized from ethylacetate and has a melting point of 132° to 133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743399
Source datasetuspto-grants-1988_05
ORD IDord-08faefba7750412dbd2f4cbd4df33ab8
Source noteuspto-grants-1988_05