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HRID 48111作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcrylateHCID 8821—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物2-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-buta-1,3-dieneHCID 20632154—
溶媒TolueneHCID 1140—
生成物4-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-cyclohex-3-enecarboxylic Acid Ethyl EsterHCID 8675936888%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703082B1
出典データセットuspto-grants-2004_03
ORD IDord-487cb1cdebea42d59d94f98259f552fc
出典メモuspto-grants-2004_03