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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441206Generated: October 31, 2026

Methacrylic Acid → HCID 86613967, compound

https://huagongshe.com/reaction/1441206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic AcidHCID 4093—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant9-AnthracenemethanolHCID 73848—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86613967HCID 86613967—

Reaction Steps

208 g of 9-anthracene methanol (1 mol), 309 g of dicyclohexyl carbodiimide (1.5 mol) and a methacrylic acid were stirred and dissolved in 2,000 g of a THF solution to form a preliminary mixture. 183 g of 4-dimethyl amino pyridine (1.5 mol) was injected into the preliminary mixture at a temperature of 0° C. to obtain a mixture. The mixture was stirred at room temperature for 6 hours. A solvent was then removed from the stirred mixture. The mixture without the solvent was repeatedly re-crystallized using methanol to obtain 163 g of an anthracene methacrylate monomer. 82 g of the anthracene methacrylate monomer, 34 g of p-tert-butoxystryne and 43 g of methacrylic acid were dissolved in 380 g of propylene glycol monomethyl ether acetate (PMA) to obtain a polymerization mixture. The polymerization mixture was heated at a temperature of 60° C. for 2 hours under a nitrogen atmosphere to synthesize a preliminary copolymer resin. 1 l of n-hexane was injected into the preliminary copolymer resin to remove non-polymerized portions from the preliminary copolymer resin, thereby synthesizing 120 g of copolymer resin. Here, the copolymer resin had a weight-average molecular weight of 5,600 and a dispersion degree of a molecular weight distribution of 2.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655389B2
Source datasetuspto-grants-2010_02
ORD IDord-bdf601ef3b2d4364bec9cbb08aa6fb12
Source noteuspto-grants-2010_02