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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384057Generated: November 2, 2026

Azobisisobutyronitrile → HCID 86757133, compound

https://huagongshe.com/reaction/1384057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
ReactantHCID 86757134HCID 86757134—
SolventTolueneHCID 1140—
ProductHCID 86757133HCID 8675713332%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258508B1
Source datasetuspto-grants-2001_07
ORD IDord-2f1015dfb2a64b0d94e158d22db25c15
Source noteuspto-grants-2001_07