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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30590생성일: 2026년 10월 25일

Triethylamine → 3-((4-(Difluoromethoxy)phenyl)ethynyl)phenol

https://huagongshe.com/reaction/30590

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물m-EthynylphenolHCID 139144—
반응물1-(Difluoromethoxy)-4-iodobenzeneHCID 2737008—
촉매Copper iodideHCID 83717—
용매DimethylformamideHCID 6228—
생성물3-((4-(Difluoromethoxy)phenyl)ethynyl)phenolHCID 59790321—

반응 단계

A solution of 4-(difluoromethoxy)phenyl iodide (4.70 g) in deoxygenated dimethylformamide was treated with trans-dichlorobis(triphenylphosphine) palladium(II) (244 mg) and copper(II) iodide 66 mg) followed by triethylamine (7.52 mL), stirred under a nitrogen atmosphere for 5min., treated with 3-hydroxyphenyl acetylene (2.467 g), stirred under nitrogen atmosphere for 16 h, poured into ethyl acetate and was washed with 0.05 N HCl and water. The organic phase was dried over MgSO4 and concentrated in vacuo. The residue was chromatographed, silica gel, 40% ethyl acetate/hexane as eluent, to afford 3-((4-(difluoromethoxy)phenyl)ethynyl)phenol as a tan solid, 5.40 g; 1H NMR (DMSO-d6): δ 9.64 (s, 1H), 7.56 (d, J=8.8 Hz, 2H), 7.27 (t, J=73.7 Hz, 1H), 7.17 (d, J=8.8 Hz, 2H), 7.16 (m, 1H), 6.94 (m, 1H), 6.86 (m, 1H), and 6.77 (m, 1H); MS (ES neg) m/z 260.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423158B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-d89ce363547847d1ae42f1a34706a5ac
출처 메모uspto-grants-2008_09