戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 736581作成日:2026年10月25日

Azobisisobutyronitrile → Norbornene styrene methyl acrylate

https://huagongshe.com/reaction/736581

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物Methyl AcrylateHCID 7294—
反応物StyreneHCID 7501—
反応物2-NorborneneHCID 10352—
反応物Ethylaluminum sesquichlorideHCID 25508—
反応物Hydrochloride methanolHCID 21893726—
溶媒TolueneHCID 1140—
生成物Norbornene styrene methyl acrylateHCID 86604939—

反応手順

Norbornene (10.5 g, 112 mmol), styrene (0.6 g, 5.6 mmol), methyl acrylate (5 mL, 56 mmol), and AIBN (0.028 g, 0.17 mmol) were charged into a 250 mL Schlenk flask and dissolved in 30 mL of toluene. Ethylaluminum sesquichloride (1.38 g, 5.6 mmol) was charged into a 100 mL flask and dissolved in 20 mL of toluene. The toluene solution of ethylaluminum sesquichloride was slowly dropped to the 250 mL Schlenk flask at −70° C. The reaction temperature was raised to room temperature while stirring the mixture for 2 hours, and then the reaction was performed at 65° C. for 12 hours. The reaction solution turned to light green in color during the reaction. After the reaction was completed, the reaction solution was slowly dropped to 3000 cc of 5% v/v HCl—MeOH to precipitate a white polymer, which was filtered through a glass filter and dried in a vacuum oven at 70° C. for 12 hours to obtain a norbornene-styrene-methyl acrylate terpolymer (7.1 g: 66.7% by weight based on the total weight of used monomers). The copolymer had a Tg of 120° C., a molecular weight (Mw) of 228,000, and Mw/Mn of 16.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07595369B2
出典データセットuspto-grants-2009_09
ORD IDord-dacbc587ff594eefbfdbe450693160b3
出典メモuspto-grants-2009_09