Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374075Generated: October 30, 2026

Indene → Indene

https://huagongshe.com/reaction/374075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndeneHCID 7219—
ReactantHCID 57212560HCID 57212560—
SolventHexaneHCID 8058—
ProductIndeneHCID 7219—
ProductMaleic AnhydrideHCID 7923—

Reaction Steps

Under agitation with the stirrer, the charge was held at the reflux temperature by heating with an external heater. Thereafter, a solution containing 27 g (0.25 mol) of indene and 410 mg of azoisobutyronitrile (AIBN) as a radical polymerization initiator was charged into the overhead dropping funnel and this solution was dripped slowly into the polymerizer over 1 h. After completion of the dripping, the reaction solution was left under reflux for 2 h until the reaction was completed. The reaction solution was thereafter returned to room temperature and gradually added to 200 ml of n-hexane in a precipitating tank (beaker with an inner capacity of 500 ml), whereupon a white precipitate of indenemaleic anhydride copolymer formed. The precipitate was separated by filtration under suction and vacuum-dried to obtain a copolymer of indene and maleic anhydride in a yield of 95 wt% as calculated from equation (1) given hereinabove.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166275
Source datasetuspto-grants-1992_11
ORD IDord-98d9915edc38496e928dc12b3ad6b245
Source noteuspto-grants-1992_11