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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843077Generated: October 26, 2026

Carbon Dioxide → 1-methyl-3-pentafluoroethyl-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/1843077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSodium HydroxideHCID 14798—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-methyl-3-pentafluoroethyl-1H-pyrazoleHCID 22972273—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuran heptaneHCID 21263495—
Product1-methyl-3-pentafluoroethyl-1H-pyrazole-5-carboxylic acidHCID 1483687619.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under an argon atmosphere, 5.00 g (25.0 mmol) of 1-methyl-3-pentafluoroethyl-1H-pyrazole are initially introduced into diethyl ether and the solution is cooled to −78° C. 11.1 ml (27.7 mmol) of 2M lithium diisopropylamide solution in tetrahydrofuran/heptane are added dropwise and, at −30° C. and with vigorous stirring, 450 g of crushed dry ice are added. When the evolution of gas has stopped, the reaction mixture is admixed with 235 ml of water and adjusted to pH 11 with 1M sodium hydroxide solution. The alkaline solution is extracted three times with ethyl acetate and then adjusted to pH 2 with 1N hydrochloric acid. The aqueous phase is extracted three times with ethyl acetate and the organic phase is dried over sodium sulphate. Distilling of the solvent on a rotary evaporator under reduced pressure gives 1.20 g of 1-methyl-3-pentafluoroethyl-1H-pyrazole-5-carboxylic acid (18%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946234B2
Source datasetuspto-grants-2015_02
ORD IDord-41c8ce546ecc4c64be692adc50335656
Source noteuspto-grants-2015_02