HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292809Generated: October 30, 2026
Water → (5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazol-4-yl)methanol
https://huagongshe.com/reaction/1292809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbaldehyde | HCID 19754692 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazol-4-yl)methanol | HCID 17862871 | 52.2% |
Reaction Steps
A solution of 7.2 g (37.0 mmoles) of 5-chloro-3-difluoromethyl-1-methyl-1H-pyrazole-4-carboaldehyde dissolved in 100 ml of methanol was cooled to 0° C. Thereto was gradually added 2.1 g (55.5 mmoles) of sodium borohydride. The mixture was stirred at room temperature for 3 hours to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The resulting organic layer was washed with an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain 3.8 g (yield: 52.1%) of (5-chloro-3-difluoromethyl-1-methyl-1H-pyrazol-4-yl)-methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07238689B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-d6c664937e5a44c08ddea4cb267a9a43 |
|---|
| Source note | uspto-grants-2007_07 |
|---|