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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1496920생성일: 2026년 10월 26일

Nitrogen → methyl (2E)-3-[4'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl]-2-propenoate

https://huagongshe.com/reaction/1496920

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참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 4-bromocinnamateHCID 816774—
반응물4-(4-Trifluoromethoxyphenyl)phenolHCID 12008734—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매1,4-DioxaneHCID 31275—
생성물methyl (2E)-3-[4'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl]-2-propenoateHCID 5475781885%

반응 단계

A solution of methyl (E)-3-(4-bromophenyl)-2-propenoate (99) (0.500 g, 2.07 mmol) and 4-(trifluoromethoxy)phenylboronic acid (44) (0.612 g, 2.97 mmol) in dioxane (40 mL) and aqueous K2CO3 (2M, 10 mL, 20 mmol) was purged with N2. Pd(dppf)Cl2 (0.050 g, 0.06 mmol) was added and the solution was refluxed under N2 for 1 h. The dioxane was removed and the residue was extracted with EtOAc, the organic fraction was dried and the solvent was removed. Column chromatography of the residue on silica gel using gradient elution (hexanes to CH2Cl2) gave methyl (2E)-3-[4′-(trifluoromethoxy)[1,1′-biphenyl]-4-yl]-2-propenoate (100) (0.567 g, 85%) as a white solid: mp 98-100° C.; 1H NMR (CDCl3) δ 7.73 (d, J=16.0 Hz, 1H), 7.56-7.63 (m, 6H), 7.30 (dd, J=8.8, 0.9 Hz, 2H), 6.48 (d, J=16.0 Hz, 1H), 3.82 (s, 3H). APCI MS m/z 323 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09198913B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-af23c11d57c3404a979a89cdabf7813c
출처 메모uspto-grants-2015_12