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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489301Generated: October 31, 2026

Butyl Methacrylate → HCID 23469697, compound

https://huagongshe.com/reaction/1489301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl MethacrylateHCID 7354—
ReactantGlycidyl methacrylateHCID 7837—
Reactant1-DodecanethiolHCID 8195—
Reactant2,2'-Azobis(2,4-dimethyl-4-methoxyvaleronitrile)HCID 85867—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23469697HCID 2346969750%

Reaction Steps

Into a 1 l four-necked flask, 25.0 g of glycidyl methacrylate, 25.0 g of n-butyl methacrylate, 10.0 g of 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile), 5.0 g of n-dodecylmercaptan and 500 ml of dioxane were charged, dissolved and stirred. Then, stirring was continued under a nitrogen stream at 70° C. for 4 hours. The reaction solution was put into methanol to precipitate the resin. Purification was repeated with tetrahydrofuran/methanol, and then vacuum drying was conducted at 40° C. to obtain a resin powder. The obtained amount was 38.0 g. The weight average molecular weight as measured by GPC was 14,000 as calculated as polystyrene; the glass transition temperature (Tg) was 33° C.; and the epoxy equivalent was 205. 25 g of a glycidyl methacrylate/n-butyl methacrylate copolymer thus obtained, 6.5 g of an epoxy-type heat-curing agent (EX-611, manufactured by Nagase Chemicals Ltd.), 1.6 g of a curing catalyst (SI-190, manufactured by Shanshin Chemical Industry Co., Ltd.) and 77 g of diethylene glycol dimethyl ether were mixed and dissolved, followed by filtration with a 0.2 μm filter to obtain a planarizing material solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677380
Source datasetuspto-grants-1997_10
ORD IDord-b79e7e8e8b814e27ab0d119efc10119f
Source noteuspto-grants-1997_10