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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48111생성일: 2026년 10월 24일

Ethyl Acrylate → 4-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-cyclohex-3-enecarboxylic Acid Ethyl Ester

https://huagongshe.com/ko/reaction/48111

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcrylateHCID 8821—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물2-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-buta-1,3-dieneHCID 20632154—
용매TolueneHCID 1140—
생성물4-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-cyclohex-3-enecarboxylic Acid Ethyl EsterHCID 8675936888%

반응 단계

To a slurry of aluminum chloride (0.1 equi) in toluene (1 mL/mmole), ethyl acrylate (1 equi.) (1 equi.) was added at ice temperature. The reaction mixture was stirred at ice temperature for 10 min. Then a solution 2-(5,5,6,6,7,7,8,8,8-nonafluoro-octyl)-buta-1,3-diene (40) (0.5M in THF) (1 equi.) was added at ice temperature over a period of 20 min. The reaction mixture was stirred at ice temperature for 10 h, water, extracted with hexane, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (hexanes) gave 4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyl)-cyclohex-3-enecarboxylic acid ethyl ester (41) as a colorless oil (88%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703082B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-487cb1cdebea42d59d94f98259f552fc
출처 메모uspto-grants-2004_03