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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 900197생성일: 2026년 10월 25일

Tetrahydrofuran → 4-(2-Vinyl-benzooxazol-5-yl)-benzonitrile

https://huagongshe.com/reaction/900197

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Tris(1,1-dimethylethyl)phosphineHCID 83681—
반응물4-Cyanophenylboronic acidHCID 2734326—
반응물5-Bromo-2-ethenyl-1,3-benzoxazoleHCID 21980099—
용매HexaneHCID 8058—
생성물4-(2-Vinyl-benzooxazol-5-yl)-benzonitrileHCID 2198009178%

반응 조건

온도23 °C

반응 단계

A mixture of 224 mg (1 mmol) of 5-bromo-2-vinyl-benzooxazole, 191 mg (1.3 mmol) of 4-cyanophenylboronic acid, 55 mg (0.03 mmol) of tris-(dibenzylidineacetone)dipalladium (0) (CAS #52409-22-0), 0.2 mL (0.06 mmol) of a 10% solution of tri-tert-butylphosphine in hexane, and 1.5 mL of tetrahydrofuran was stirred at 23° C. for 24 hours. It was then heated at 65° C. for 0.5 hour, then cooled. The mixture was suction filtered to remove particulates, then partitioned between 80 mL of water and a mixture of 30 mL of ethyl acetate and 10 mL of hexane. The organic phase was collected, dried over Na2SO4, and purified by flash chromatography on silica gel (eluting with 1:1 hexane: dichloromethane) to give 4-(2-vinyl-benzooxazol-5-yl)-benzonitrile (192 mg, 78%) as a white solid: mp 143-144° C.; 1H NMR (300 MHz, CDCl3) δ 7.90 (d, J=1.8 Hz, 1 H), 7.76 (d, J=8.4 Hz, 2 H), 7.70 (d, J=8.4 Hz, 2 H), 7.62 (d, J=7.5 Hz, 1 H), 7.55 (dd, J=7.5, 1.8 Hz, 1 H), 6.79 (dd, J=17.4, 10.5 Hz, 1 H), 6.52 (d, J=17.4 Hz, 1 H), 5.91 (d, J=10.5 Hz, 1 H); Mass spectrum: [M+H]+ 247.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07358263B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-f067bccacd414f35aa5456558863f988
출처 메모uspto-grants-2008_04