돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48110생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물2-(Benzyloxy)-6-bromonaphthaleneHCID 640595—
반응물4-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyloxy)-tosylateHCID 86759366—
촉매copper(I) bromideHCID 24593—
용매TetrahydrofuranHCID 8028—
생성물2-(5,5,6,6,7,7,8,8,8-Nonafluoro-octyl)-buta-1,3-dieneHCID 20632154—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703082B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-b0fae634104f4e8badaca1a75ce245db
출처 메모uspto-grants-2004_03