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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40934생성일: 2026년 10월 24일

Pyridine → 1-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

https://huagongshe.com/ko/reaction/40934

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DimethylformamideHCID 6228—
반응물Phenylboronic AcidHCID 66827—
반응물4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2774010—
촉매Cupric acetateHCID 8895—
용매Ethyl AcetateHCID 8857—
생성물1-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 56965771—

반응 조건

온도80 °C

반응 단계

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.07 g, 0.0003 mol) and phenylboronic acid (0.083 g, 0.00068 mol) were combined in DMF (1.50 mL, 0.0194 mol). Then copper(II) diacetate (0.010 g, 0.000055 mol) and pyridine (0.069 mL, 0.00085 mol) were added. The reaction was heated in an open tube to 80° C. for 40 minutes. The reaction was complete by HPLC, allowed to cool to rt, taken up in ethyl acetate, and washed with water saturated with sodium carbonate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated to give 1-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazo, 0.09 gm as an oily residue, LC/MS (M+H)+: 271.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530485B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-dcf8f8518fa74b658934c37d9471e542
출처 메모uspto-grants-2013_09