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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740696Generated: October 26, 2026

Indene → Isopropenyltoluene indene

https://huagongshe.com/reaction/1740696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndeneHCID 7219—
ReactantSodium HydroxideHCID 14798—
ReactantO,alpha-dimethylstyreneHCID 81886—
ProductIsopropenyltoluene indeneHCID 86585515—

Reaction Steps

Isopropenyltoluene, indene, dehydrated and purified toluene, and a boron trifluoride phenolate complex (1.6-times equivalent of phenol) diluted to 10-times volume with dehydrated and purified toluene were continuously supplied to an autoclave having a net capacity of 1270 ml equipped with a stirring blade, so that the ratio by mol of isopropenyltoluene to indene was 80/20 and the total supplied amount of isopropenyltoluene and indene was 1.0 l/h. The mixture was polymerized at a reaction temperature of 5° C. Subsequently, the reaction mixture was transferred to a second-stage autoclave and the polymerization reaction was continued at 5° C. Then, when the total retention time in the first- and second-stage autoclaves reached 2 hours, the reaction mixture was discharged continuously. After a period of time three times the retention time had elapsed, the polymerization reaction was completed. After completion of the polymerization, an aqueous 1N NaOH solution was added to the reaction mixture to terminate the polymerization reaction. The resulting reaction mixture was washed with large amounts of water five times; then, the solvent and unreacted monomers were distilled off under reduced pressure by an evaporator to obtain an isopropenyltoluene/indene copolymer (2). This copolymer had a softening point Tm of 90° C., a number average molecular weight Mn of 680, and a weight average molecular weight Mw of 980.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972547
Source datasetuspto-grants-1999_10
ORD IDord-1716cbd1fc404d50ab9ee96df60b1486
Source noteuspto-grants-1999_10