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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7686생성일: 2026년 10월 24일

Potassium Carbonate → [4-(1,3-Benzoxazol-2-yl)-2-methylphenyl]acetonitrile

https://huagongshe.com/ko/reaction/7686

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참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물TriphenylphosphineHCID 11776—
반응물Methylboronic AcidHCID 139377—
반응물[4-(1,3-Benzoxazol-2-yl)-2-bromophenyl]acetonitrileHCID 10236618—
촉매HCID 178418476HCID 178418476—
용매Water 1,2-dimethoxyethaneHCID 18180031—
생성물[4-(1,3-Benzoxazol-2-yl)-2-methylphenyl]acetonitrileHCID 10214599—

반응 조건

온도80 °C

반응 단계

A mixture of methane boronic acid (57.6 mg, 0.96 mmol), [4-(1,3-benzoxazol-2-yl)-2-bromophenyl]acetonitrile (example 1) (200 mg, 0.64 mmol), dichlorobis(triphenylphosphine)palladium(II) (22.4 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 80° 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 a brown solid. Purification of the crude solid by flash chromatography on silica gel eluting with a gradient of EtOAc:hexanes (0 to 40 min: 0 to 25% EtOAc) afforded the desired [4-(1,3-benzoxazol-2-yl)-2-methylphenyl]acetonitrile as a yellow solid. 1H NMR (CDCl3, 300 MHz) δ 8.14 (s, 1H), 8.11 (d, 1H), 7.78 (m, 1H), 7.60 (m, 1H), 7.54 (d, 1H), 7.38 (m, 2H), 3.76 (s, 2H), 2.45 (s, 3H). MS (ESI) 249 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-99598980dcbc49b2980aba4c026922bd
출처 메모uspto-grants-2006_08