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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57091생성일: 2026년 10월 24일

Ethyl Acetate → 3-(3-chloro-1H-pyrazol-1-yl)pyridine

https://huagongshe.com/ko/reaction/57091

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물3-Chloro-1-(pyridine-3-yl)-1H-pyrazole-5-carboxylic acid hydrochlorideHCID 118021782—
촉매Copper oxideHCID 14829—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ammonium HydroxideHCID 14923—
생성물3-(3-chloro-1H-pyrazol-1-yl)pyridineHCID 6749954073.4%

반응 조건

온도120 °C

반응 단계

3-Chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid hydrochloride (1.00 g, 3.65 mmol) was stirred in N,N-dimethylformamide (10 mL). Copper(II) oxide (58.0 mg, 0.730 mmol) was added and the reaction was heated at 120° C. for 16 hours, at which point the reaction was ˜20% complete. Additional copper(II) oxide (112 mg, 1.46 mmol) was added and the reaction was stirred for 5 hours, at which point the reaction was complete by thin layer chromatography (TLC) [Eluent: ethyl acetate]. The mixture was diluted with ammonium hydroxide (NH4OH) and water and extracted with ethyl acetate. The organic layer was washed with 15% lithium chloride and concentrated to provide an orange solid. The residue was purified by flash column chromatography using ethyl acetate as eluent and the pure fractions were concentrated to afford the desired product as a white solid (481 mg, 69.7%). The spectral characterization was in agreement with the product prepared previously.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434712B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-e057a9d09fff4e41a0af34e569f9968e
출처 메모uspto-grants-2016_09