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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2427021생성일: 2026년 10월 23일

Carbon Dioxide → 1-Methyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/ko/reaction/2427021

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Sodium HydroxideHCID 14798—
반응물Lithium diisopropylamideHCID 2724682—
반응물1-Methyl-3-(trifluoromethyl)-1H-pyrazoleHCID 2780404—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매Tetrahydrofuran heptane ethylbenzolHCID 22742125—
생성물1-Methyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acidHCID 606540—

반응 조건

온도-78 °C

반응 단계

To a mixture of 8.71 g of 1-methyl-3-trifluoromethyl-1H-pyrazole and 130 ml of tetrahydrofuran was added dropwise 32 ml of a 2.0 mol/L lithium diisopropylamide solution in heptane/tetrahydrofuran/ethylbenzene at −78° C. The mixture of stirred at −78° C. for 2 hours and then poured into a mixture was dry ice and 50 ml of tetrahydrofuran. The mixture was stirred for 2 hours while allowing it to rise to around room temperature. Water and diethyl ether were poured into the reaction mixture. The aqueous layer was adjusted to pH 10-12 by an addition of a 2N aqueous sodium hydroxide solution, and then layers were separated. The resulting aqueous layer was washed with diethyl ether two times, adjusted to around pH 3 by an addition of 2N hydrochloric acid, and then extracted with methyl tert-butyl ether three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over magnesium sulfate, and concentrated under reduced pressure to obtain 8.19 g of 1-methyl-3-trifluoromethyl-1H-pyrazole-5-carboxylic acid of the formula:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07968573B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-14b4666279644e6d9d5b8faa2192b973
출처 메모uspto-grants-2011_06