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HRID 251911作成日:2026年10月27日

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

https://huagongshe.com/reaction/251911

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Sodium HydroxideHCID 14798—
反応物Lithium diisopropylamideHCID 2724682—
反応物1-Methyl-3-(trifluoromethyl)-1H-pyrazoleHCID 2780404—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒Tetrahydrofuran heptane ethylbenzolHCID 22742125—
生成物1-Methyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acidHCID 606540—

反応条件

温度-78 °C

反応手順

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:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07867949B2
出典データセットuspto-grants-2011_01
ORD IDord-68f523613179463c93cc9b87b047c609
出典メモuspto-grants-2011_01