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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30557생성일: 2026년 10월 24일

1-(Difluoromethoxy)-4-ethynylbenzene → 1-Butyl-3-{[4-(difluoromethoxy)phenyl]ethynyl}benzene

https://huagongshe.com/ko/reaction/30557

반응식

참여 물질

역할이름HCID투입량
반응물1-(Difluoromethoxy)-4-ethynylbenzeneHCID 2778497—
반응물1-Bromo-3-butylbenzeneHCID 13954102—
생성물1-Butyl-3-{[4-(difluoromethoxy)phenyl]ethynyl}benzeneHCID 57435860—

반응 단계

Using essentially the same procedure described in Example 1, step a, and employing 1-bromo-3-butylbenzene and 1-(difluoromethoxy)-4-ethynylbenzene, the phenylethynylbenzene product was obtained. This product was purified on silica gel (Biotage) using hexanes/EtOAc 50/1 as the eluting solvents to give 1-butyl-3-{[4-(difluoromethoxy)phenyl]ethynyl}benzene as a colorless oil (0.56 g, 28% yield), MS m/e M+ 300; 1H NMR (400 MHz, DMSO-d6) 0.82 (t, J=7.19 Hz, 3H), 1.25 (m, 2H), 1.55 (m, 2H), 2.56 (t, J=7.56 Hz, 2H), 7.2 (m, 3H), 7.35-7.45 (m, 4H), 7.58 (d, J=8.79 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423158B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-ef3dcaa71b4b406faed3b6f663c3af0f
출처 메모uspto-grants-2008_09