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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230906Generated: October 30, 2026

Hydrochloric Acid → HCID 86584203, compound

https://huagongshe.com/reaction/2230906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
Reactant1,3-ButadieneHCID 7845—
Reactant1,3-CyclohexadieneHCID 11605—
SolventMethanolHCID 887—
ProductHCID 86584203HCID 86584203—

Reaction Steps

The catalyst B (18 mg, 0.1 mmol) previously synthesized was dissolved into 15 ml of toluene at room temperature under an argon atmosphere in a Schlenck tube, and then 1.8 ml of a toluene solution (aluminum: 10 atomic %) of methyl aluminoxane which is a co-catalyst was added thereto so as to adjust a catalyst solution. In the meantime, 1,3-cyclohexadiene (8 g, 0.1 mol) and butadiene (10.8 g, 0.2 mol) as monomers were dissolved into 15 ml of toluene at room temperature under an argon atmosphere. While this solution was kept to room temperature and was stirred, the total amount thereof was added to the total amount of the above-mentioned catalyst solution. Polymerization advanced promptly and the reaction finished within 30 minutes. A slurry containing the produced polymer was added to a great deal of methanol acidified with hydrochloric acid to precipitate and isolate the polymer. Methanol was then removed by filtration. The resultant was vacuum-dried at room temperature for 24 hours to obtain a cyclohexadiene-butadiene copolymer. The yield of the polymer was 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426396B2
Source datasetuspto-grants-2002_07
ORD IDord-c4a381986ecd4beaa521d5e6c8abc394
Source noteuspto-grants-2002_07