돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43992생성일: 2026년 10월 23일

Potassium Carbonate → 3-(3-Nitropyridin-4-yl)benzoic acid

https://huagongshe.com/ko/reaction/43992

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-Carboxyphenylboronic acidHCID 2733957—
반응물4-Chloro-3-nitropyridineHCID 2735781—
용매1,4-DioxaneHCID 31275—
생성물3-(3-Nitropyridin-4-yl)benzoic acidHCID 59233790—

반응 조건

온도100 °C

반응 단계

To a degassed mixture containing 4-chloro-3-nitropyridine (3.0 g, 18.9 mmol), 3-boronobenzoic acid (3.7 g, 22.7 mmol), potassium carbonate (5.2 g, 37.8 mmol) and dioxane (189 mL) was added tetrakis(tiphenylphosphine)palladium(0) (0.30 g, 0.28 mmol) in one portion under a nitrogen atmosphere. The mixture was heated with fast stirring at 100° C. for 15 h, cooled to room temperature, filtered and concentrated to afford 3-(3-nitropyridin-4-yl)benzoic acid as a tan residue which was used without further purification. LCMS: retention time: 1.375 min. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Waters-Sunfire, 5u, C18, 4.6×50 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 4 mL/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 3 min, a hold time of 1 min, and an analysis time of 4 min where solvent A was 10% CH3CN/90% H2O/10 mM TFA and solvent B was 10% H2O/90% CH3CN/10 mM TFA. MS data was determined using a Micromass Platform for LC in electrospray mode. m/z 245 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536338B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-f3364d1d09824350b9e5f65f603e50d3
출처 메모uspto-grants-2013_09