HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384057Generated: November 2, 2026
Azobisisobutyronitrile → HCID 86757133, compound
https://huagongshe.com/reaction/1384057
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | HCID 86757134 | HCID 86757134 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86757133 | HCID 86757133 | 32% |
Reaction Steps
1 g (0.0017 mole) of t-butyl 3α-(5-norbornene-2-carbonyloxy)-7α, 12α-dihydroxy-5β-cholan-24-oate prepared in Example 4, 0.17 g (0.0017 mole) of purified maleic anhydride, and 0.0056 g (2 mole %) of 2,2′-azobisisobutyronitrile as a radical polymerization initiator, were dissolved in 3 ml of toluene solvent. The solution was introduced into a polymerization glass tube ampule which was then sealed under vacuum. Then, the solution was polymerized at a temperature of 65° C. for 20 hours. After the polymerization, the polymerization product was precipitated in petroleum ether/ethyl ether(5/1, volume ratio), and the precipitate was recovered with a glass filter. The recovered material was dried under vacuum at a temperature of 40° C. for 12 hours, thereby obtaining 0.37 g (32% yield) of poly(t-butyl 3α-(5-norbornene-2-carbonyloxy)-7α, 12α-dihydroxy-5β-cholan-24-oate-maleic anhydride), as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258508B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-2f1015dfb2a64b0d94e158d22db25c15 |
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| Source note | uspto-grants-2001_07 |
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