HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703742Generated: November 1, 2026
Azobisisobutyronitrile → HCID 173649, compound
https://huagongshe.com/reaction/1703742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 1-Hexene | HCID 11597 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 173649 | HCID 173649 | — |
Reaction Steps
A separable flask fitted with a reflux condenser was charged with 98 parts of maleic anhydride, 300 parts of methyl ethyl ketone, 84 parts of hexene-1 and 4 parts of azobisisobutyronitrile, and the mixture was reacted with stirring in an atmosphere of nitrogen at 65°-70° C. After carrying out the reaction for 10 hours, the system was cooled to room temperature and cold methanol was added to precipitate a polymer, which was separated, collected and dried under reduced pressure to obtain 108 parts of a hexene-1-maleic anhydride copolymer (mol ratio 1:1, MW = 3800). A mixture of 91 parts of the so obtained copolymer and 400 parts of a 10% aqueous sodium hydroxide solution was stirred at 80°-90° C. to obtain an aqueous solution of a water-soluble hexene-1-sodium maleate copolymer (hereinafter referred to as water-soluble salt (II-2) or Na salt of (C6 -MA) copolymer).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04125410 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-4cbc0b6dd5984b13bb62b12e808baf50 |
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| Source note | uspto-grants-1978_11 |
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