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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542553Generated: October 25, 2026

Oxygen → Styrene

https://huagongshe.com/reaction/542553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantBenzoyl PeroxideHCID 7187—
ReactantStyreneHCID 7501—
ReactantFenobucarbHCID 19588—
SolventMethanolHCID 887—
ProductStyreneHCID 7501—
ProductDioxidan-2-idecarboxylateHCID 15793132—

Reaction Steps

A glass ampoule having an inner volume of 20 ml was filled with 2.08 g of BPMC (purity 96.0% by weight), 8.0 g of refined styrene, and 0.1 g of benzoyl peroxide (purity 99.8% by weight), displaced with nitrogen gas, and then sealed by fusion. This ampoule was kept immersed in a constant oil bath at 100° C. for one hour. Then, the ampoule was taken out of the bath, cooled, and opened. The reaction product was dropped into 500 ml of methanol and allowed to precipitate therein. The white solid consequently formed was separated by filtration and dried under a vacuum. The product consequently obtained weighed 5.8 g. The active oxygen content of the product was found to be 1.20%. In the infrared absorption spectrum of this product, absorptions by carbonyl group were observed at 1725 and 1795 cm-1 and a characteristic absorption by benzene ring was observed below 1600 cm-1. The data indicate that the white solid was a copolymer formed of styrene structural units and peroxycarbonate structural units. The conditions of copolymerization and the analyses of the produced copolymer are shown in Table 4A and the data on the copolymer's stability of storage are shown in Table 7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04658001
Source datasetuspto-grants-1987_04
ORD IDord-81083656c1ae470bb30bdf829c27fa66
Source noteuspto-grants-1987_04