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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7760생성일: 2026년 10월 24일

Ethyl Acetate → 5-(1,3-Benzoxazol-2-yl)-2-pyridin-2-yl benzonitrile

https://huagongshe.com/ko/reaction/7760

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물2-(Tributylstannyl)pyridineHCID 607784—
반응물4-(1,3-Benzoxazol-2-yl)-2-cyanophenyl trifluoromethanesulfonateHCID 21990967—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
용매Sodium chloride; waterHCID 57417360—
생성물5-(1,3-Benzoxazol-2-yl)-2-pyridin-2-yl benzonitrileHCID 10236467—

반응 조건

온도90 °C

반응 단계

The degassed solution of 4-(1,3-benzoxazol-2-yl)-2-cyanophenyl trifluoromethanesulfonate (300 mg, 1.2 mmol) in DME (5 mL) was added 2-tri-n-butylstannylpyridine (273 mg, 0.74 mmol), tetrakis(triphenylphosphine)palladium(0) (150 mg, 0.1 mmol). The reaction was stirred at 90° C. overnight and cooled to rt. EtOAc (100 mL) was added, as well as brine (50 mL). The organic layer was washed with brine (2×20 mL), dried (MgSO4), and the crude material was purified on flash column (silica gel, hexanes:EtOAc 3:1) to afford desired 5-(1,3-benzoxazol-2-yl)-2-pyridin-2-yl benzonitrile as pinkish solid. 1H NMR (CD3OD, 300 MHz), δ 8.85 (d 1H), 8.72 (d, 1H), 8.59 (m, 1H), 8.08 (d, 1H), 7.91 (d, 2H), 7.85 (m, 1H), 7.65 (m, 1H), 7.45 (m, 3H). MS (ESI) 298 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-2b86ba7fc6984a3c8299ef5961aa3279
출처 메모uspto-grants-2006_08