Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Fenobucarb | HCID 19588 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Styrene | HCID 7501 | — |
| Product | Dioxidan-2-idecarboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04658001 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-81083656c1ae470bb30bdf829c27fa66 |
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| Source note | uspto-grants-1987_04 |
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