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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396109Generated: October 30, 2026

Maleic Anhydride → HCID 131724028, compound

https://huagongshe.com/reaction/396109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
ReactantHCID 23002963HCID 23002963—
ReactantHCID 23448537HCID 23448537—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131724028HCID 13172402850%

Reaction Steps

2.57 g (0.01 mol) of 2-(2-trimethylsilyl-2-propyl)carbonyloxy-5-norbornene obtained in Example 3, 1.0 g (0.01 mol) of purified maleic anhydride, 1.36 g (0.006 mol) of (2-trimethylsilyl-2-propyl)methacrylate, and 0.067 g (1.5 mole %) 2,2-azobisisobutyronitrile as a radical initiator are added to a polymerization flask. The mixture is dissolved in 3.2 g of purified tetrahydrofuran and is polymerized at 65° C. for 24 hours under nitrogen atmosphere. After the polymerization, polymerization product is precipitated with methanol, is saved by a glass filter, and is then dried at 40° C. for 12 hours to give 2.47 g of copolymer 2-(2-trimethylsilyl-2-propyl)carbonyloxy -5-norbornene-maleic anhydride-(2-trimethylsilyl-2-propyl)methacrylate (yield 50%) as a white solid. Mn is 6,520 and glass transition temperature is not observed. The 1H-NMR spectrum in FIG. 7 showed the synthesis of a copolymer with desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06607867B1
Source datasetuspto-grants-2003_08
ORD IDord-0c42267478de4080940e37f36dd363a3
Source noteuspto-grants-2003_08