HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652702Generated: October 30, 2026
Azobisisobutyronitrile → HCID 22904624, compound
https://huagongshe.com/reaction/652702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-vinyl-2-pyrrolidone | HCID 6917 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22904624 | HCID 22904624 | — |
Reaction Steps
Copoly(N-vinyl-2-pyrrolidone/maleic anhydride was prepared as follows. About 7.8 g of maleic anhydride was added to about 85 ml of dioxane in a flask equipped with a reflux condenser, mechanical stirrer, and nitrogen inlet. The flask and its contents were heated to about 80° C. About 7.06 g of N-vinyl-2-pyrrolidone and about 0.96 g azobisisobutyronitrile were dissolved in about 50 ml of dioxane. About 15 ml aliquots of the N-vinyl-2-pyrrolidone solution were added to the contents of the flask at 15 minute intervals, while maintaining the temperature of the flask at about 80° C. After addition was complete, the flask was held at about 80° C. to provide for a total reaction time of 3 hours. The reaction mixture was cooled to room temperature, poured into about 250 ml of petroleum ether, to precipitate the polymer, and filtered. The solid product was dried, and inhibition of calcium orthophosphate scale was determined as described above. The results are reported in Table 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04673508 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-82de0c5e51734daaa5be66346d70a788 |
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| Source note | uspto-grants-1987_06 |
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