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HRID 48110作成日:2026年10月23日

2-(Benzyloxy)-6-bromonaphthalene → 2-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-buta-1,3-diene

https://huagongshe.com/ja/reaction/48110

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Benzyloxy)-6-bromonaphthaleneHCID 640595—
反応物4-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyloxy)-tosylateHCID 86759366—
触媒copper(I) bromideHCID 24593—
溶媒TetrahydrofuranHCID 8028—
生成物2-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-buta-1,3-dieneHCID 20632154—

反応手順

To a solution of 4-(5,5,6,6,7,7,8,8,8-nonafluoro-octyl)-tosylate (10), (1 equi) and copper (I) bromide (0.05 equi.) in THF (2 mL/mmole), a solution of buta-1,3-diene-2-magnesium chloride, prepared as described in (3), (38) (0.5M in THF) (1.3 equi.) was added at ice temperature over a period of 20 min. The reaction mixture was stirred at room temperature for 24 h, quenched with 5% aqueous ammonium chloride (1 mL/mmole), extracted with hexane, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (hexane) gave 2-(5,5,6,6,7,7,8,8,8-nona fluoro-octyl)-buta-1,3-diene (39) a colorless oil (96%).

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-b0fae634104f4e8badaca1a75ce245db
出典メモuspto-grants-2004_03