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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57082생성일: 2026년 10월 24일

Tetrahydrofuran → methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/ko/reaction/57082

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Ceric ammonium nitrateHCID 180504—
반응물Methyl 3-chloro-1-(pyridine-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylateHCID 118022669—
용매WaterHCID 962—
생성물methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylateHCID 118022666—

반응 단계

In step b of Scheme 2, methyl 3-chloro-1-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylate (6c) is oxidized with diammonium cerium (IV) nitrate (CAN) in water and polar solvents such as tetrahydrofuran at temperatures from about 0° C. to about 30° C. to yield methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate (6d). It was surprisingly discovered that the oxidation in step b can also proceed with potassium permanganate (KMnO4) as the oxidant in polar solvents such as acetone at temperatures from about 0° C. to about 30° C. However, many standard oxidation procedures such as, for example potassium persulfate (K2S2O8), iodine pentoxide (I2O5), copper oxide (CuO), and hydrogen peroxide were found to be inoperative.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434712B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-b97d2d1d8aee4941b85b5295b8212e23
출처 메모uspto-grants-2016_09