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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-methyl-3-pentafluoroethyl-1H-pyrazole | HCID 22972273 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran heptane | HCID 21263495 | — |
| Product | 1-methyl-3-pentafluoroethyl-1H-pyrazole-5-carboxylic acid | HCID 14836876 | 19.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946234B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-41c8ce546ecc4c64be692adc50335656 |
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| Source note | uspto-grants-2015_02 |
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