HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → N-tert-Butyl-3,5-di(difluoromethyl)-4-pyrazolecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-tert-Butyl-3,5-di(difluoromethyl)-4-pyrazolecarboxylic acid ethyl ester | HCID 71770124 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-tert-Butyl-3,5-di(difluoromethyl)-4-pyrazolecarboxylic acid | HCID 71770373 | 97.4% |
Reaction Steps
N-tert-Butyl-3,5-di(difluoromethyl)-4-pyrazolecarboxylic acid ethyl ester (3.40 g, 11.5 mmol) in ethanol (23 ml) was admixed gradually with an 8N aqueous sodium hydroxide solution (4.3 ml) and stirred at room temperature for 3 h. The solvent was removed by rotary evaporation; the residue was taken up in water (40 ml) and extracted with diethyl ether (20 ml). Acidification to pH 1 with 6M HCl was followed by extraction with ethyl acetate (3×30 ml). The combined organic phases were dried over sodium sulphate and filtered, and the solvent was removed by rotary evaporation. N-tert-Butyl-3,5-di(difluoromethyl)-4-pyrazolecarboxylic acid (3.0 g, 11.2 mmol, 97%) was isolated as a pale reddish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309202B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-cb0fc5017ba544bd87e323219bdac265 |
| Source note | uspto-grants-2016_04 |