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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1670465생성일: 2026년 10월 26일

Sodium Carbonate → 3-(3,5-Dichlorophenyl)pyridine

https://huagongshe.com/reaction/1670465

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참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물Benzene, 1-bromo-3,5-dichloro-HCID 29766—
반응물3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 2734656—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물3-(3,5-Dichlorophenyl)pyridineHCID 57699421114.2%

반응 조건

온도80 °C

반응 단계

Synthesized according to General Procedure 36. A mixture of 1-bromo-3,5-dichloro-benzene (424 mg, 1.88 mmol), 3-pyridineboronic acid pinacol ester (500 mg, 2.44 mmol), aqueous 2M Na2CO3 (1.96 mL, 3.93 mmol) and Pd(PPh3)4 (89 mg, 4 mol %) in anhydrous toluene (18 mL) was stirred overnight at 80° C. under nitrogen. The reaction was cooled down to room temperature, diluted with water (5 ml) and ethyl acetate (10 ml). The organic phase was separated, dried (Na2SO4), filtered and concentrated under reduced pressure to give a pale yellow oil, which was purified by silica-gel column chromatography to give 3-(3,5-dichlorophenyl)pyridine (481 mg, 74%) as a white solid. 1H-NMR (400 MHz, CDCl3) δ 8.81 (d, J=2.1 Hz, 1H), 8.65 (dd, J=1.4, 4.8 Hz, 1H), 7.85-7.82 (m, 1H), 7.46 (d, J=1.8 Hz, 2H), 7.41-7.38 (m, 2H). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=224.3; tR=1.21 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07994166B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-a2c415552ea54940a8c385187750ed78
출처 메모uspto-grants-2011_08