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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15523생성일: 2026년 10월 24일

Ethanol → 6-(4-Fluorophenyl)picolinic acid

https://huagongshe.com/ko/reaction/15523

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물6-Bromopyridine-2-carboxylic acidHCID 593919—
반응물2-(4-Fluorophenyl)-5,5-dimethyl-1,3,2-dioxaborinaneHCID 11020077—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물6-(4-Fluorophenyl)picolinic acidHCID 2108170846%

반응 조건

온도100 °C

반응 단계

A solution of 6-bromopicolinic acid (Aldrich) (2.02 g, 10 mmol) in DME containing 4 mL of 10% aq Na2CO3 was purged with Ar gas. To this mixture was added Pd(PPh3)4 followed by 2-(4-fluorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane (2.40 g, 11.5 mmol, Wako Pure Chemical Industries, Ltd) and EtOH (20 mL), and the mixture was purged with Ar gas. The reaction mixture was heated at 100° C. for 2.5 h in a sealed tube. Additional 2-bromopicolinic acid (900 mg) and Pd (OAc)2 was added, and after purging with Ar gas it was heated at 100° C. for 4.5 h. Trifluoroacteic acid (20 mL) was added to the reaction mixture, concentrated and MeOH (150 mL) was added to the residue. The insoluble material was filtered, and the filtrate solution was concentrated. Purification by flash column on silica gel eluting with EtOAc/MeOH//900:100 followed by EtOAc/MeOH/HOAc//700:1500:50 provided the desired product (1.0 g, 40% based on borinane starting material) as a white solid. 1H NMR (CD3OD) δ 8.01 (d, 1H, J=7.7 Hz), 7.94-7.87 (m, 3H), 7.73 (d, 1H, J=7.7 Hz), 7.13 (t, 2H, 8.8 Hz); MS(ESI+) m/z 234 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732613B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b3ac16c53b60473596afcd58d309504e
출처 메모uspto-grants-2010_06