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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7685생성일: 2026년 10월 23일

Potassium Carbonate → [5-(1,3-Benzoxazol-2-yl)-2',4'-dimethoxy-1,1'-biphenyl-2-yl]acetonitrile

https://huagongshe.com/ko/reaction/7685

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물TriphenylphosphineHCID 11776—
반응물2,4-Dimethoxybenzeneboronic acidHCID 2734341—
반응물[4-(1,3-Benzoxazol-2-yl)-2-bromophenyl]acetonitrileHCID 10236618—
촉매HCID 178418476HCID 178418476—
용매Water 1,2-dimethoxyethaneHCID 18180031—
생성물[5-(1,3-Benzoxazol-2-yl)-2',4'-dimethoxy-1,1'-biphenyl-2-yl]acetonitrileHCID 10287076—

반응 조건

온도83 °C

반응 단계

A mixture of 2,4-dimethoxyphenylboronic acid (175 mg, 0.96 mmol), [4-(1,3-benzoxazol-2-yl)-2-bromophenyl]acetonitrile (example 1) (200 mg, 0.64 mmol), dichlorobis(triphenylphosphine)palladium(II) (22 mg, 0.032 mmol), triphenylphosphine (17 mg, 0.064 mmol), and potassium carbonate (177 mg, 1.3 mmol) in degassed DME/H2O (5:1, 12 mL) was heated at 83° C. for 18 h. The mixture was cooled to rt, the two layers were separated and the aqueous layer was extracted with EtOAc (3×). The organics were combined, dried over Na2SO4 and evaporated to dryness to give an orange solid. Purification of the crude by flash chromatography on silica gel eluting with a gradient of EtOAc:hexanes (0 to 40 min: 0 to 20% EtOAc, 40 to 50 min: 50% EtOAc) afforded [5-(1,3-benzoxazol-2-yl)-2′,4′-dimethoxy-1,1′-biphenyl-2-yl]acetonitrile as a yellow solid. 1H NMR (CDCl3, 300 MHz) δ 8.26 (dd, 1H), 8.15 (s, 1H), 7.77 (m, 1H), 7.70 (d, 1H), 7.57 (m, 1H), 7.36 (m, 2H), 7.16 (d, 1H), 6.62 (dd, 1H), 6.57 (s, 1H), 3.88 (s, 3H), 3.78 (s, 3H), 3.64 (q, 2H). MS (ESI) 371 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7014225eb7f34ab1bb1c055274cb3365
출처 메모uspto-grants-2006_08