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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 924613생성일: 2026년 10월 25일

Tetrahydrofuran → 1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl Chloride

https://huagongshe.com/reaction/924613

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물3-chloro-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)pyridineHCID 17976291—
반응물HCID 178418918HCID 178418918—
생성물1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl ChlorideHCID 1844692884.6%

반응 조건

온도-5 °C

반응 단계

In a reaction vessel equipped with a thermometer, septum, nitrogen inlet and stirring bar, 500 mg (2.02 mmol) of 1-(3-chloro-2-pyridyl)-3-trifloromethyl-1H-pyrazole were dissolved in 3 ml of dry tetrahydrofuran. By means of a syringe, 2.0 ml of a 2 M solution of isopropyl magnesium chloride in tetrahydrofuran were added dropwise with stirring, while cooling the vessel with an ice bath and keeping the internal temperature at about 20° C. The ice bath was removed and the mixture was stirred for further 20 minutes at 23° C. Then the mixture was cooled again to −5° C. and 4.25 ml of a 20% (w/w) solution of phosgene in toluene were added dropwise with stirring. The mixture was allowed to war at 23° C. and stirred for further 1 h at 23° C. The thus obtained reaction mixture was evaporated to dryness, redissolved in toluene and stirred for further 30 min. at 50° C. Solids were removed by filtration and washed with toluene. The combined filtrates were evaporated to dryness to yield 0.53 g of the title compound with a purity >85% (yield 84.6%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09282741B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-d18ce0b8da7243d4be596d7660e86b7b
출처 메모uspto-grants-2016_03