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HRID 736581생성일: 2026년 10월 23일

Azobisisobutyronitrile → Norbornene styrene methyl acrylate

https://huagongshe.com/ko/reaction/736581

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물Methyl AcrylateHCID 7294—
반응물StyreneHCID 7501—
반응물2-NorborneneHCID 10352—
반응물Ethylaluminum sesquichlorideHCID 25508—
반응물Hydrochloride methanolHCID 21893726—
용매TolueneHCID 1140—
생성물Norbornene styrene methyl acrylateHCID 86604939—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07595369B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-dacbc587ff594eefbfdbe450693160b3
출처 메모uspto-grants-2009_09