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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81033생성일: 2026년 10월 25일

Potassium Phosphate, Tribasic → 3-Chloro-5-(4-phenoxyphenyl)isonicotinonitrile

https://huagongshe.com/reaction/81033

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물4-Phenoxyphenylboronic acidHCID 2734377—
반응물3,5-Dichloropyridine-4-carbonitrileHCID 11137599—
촉매palladium(II) acetateHCID 167845—
촉매Bis(ditert-butyl(cyclopenta-2,4-dien-1-yl)phosphane);iron(2+)HCID 12976736—
용매1,4-DioxaneHCID 31275—
생성물3-Chloro-5-(4-phenoxyphenyl)isonicotinonitrileHCID 6692691355%

반응 단계

A mixture of 3,5-dichloroisonicotinonitrile (10.00 g, 57.8 mmol), 4-phenoxyphenylboronic acid (12.37 g, 57.8 mmol), palladium(II) acetate (0.389 g, 1.734 mmol), potassium phosphate (30.7 g, 145 mmol) and 1,1′-bis(di-t-butylphosphino)ferrocene (0.833 g, 1.734 mmol) was pumped and backfilled with nitrogen 3 times. Dioxane (200 mL) was added. The reaction vial was again pumped and backfilled with nitrogen 3 times, sealed and heated to gentle reflux for 20 h. The dioxane solvent was evaporated in vacuo. The residue was diluted with water (150 mL) and brine (150 mL) and extracted with ethyl acetate (3×100 mL). The combined extracts were washed with brine (25 mL), dried (MgSO4) and concentrated. Silica gel chromatography, eluting with 0-15% ethyl acetate in dichloromethane-hexanes (1:2), gave 3-chloro-5-(4-phenoxyphenyl)isonicotinonitrile as tan liquid (9.71 g, 55% yield). 1H NMR (500 CDCl3) δ ppm 8.74 (1H, s), 8.70 (1H, s), 7.50-7.59 (2H, m), 7.35-7.46 (2H, m), 7.20 (1H, t, J=7.42 Hz), 7.06-7.16 (4H, m); MS (ES+) m/z: 307 (M+H); LC retention time: 4.298 min (analytical HPLC Method A).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846673B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-200c62f12535436abf0e038c889c3582
출처 메모uspto-grants-2014_09