HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172094Generated: October 25, 2026
Water → (5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol
https://huagongshe.com/reaction/1172094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-chloro-1-phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde | HCID 1479052 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol | HCID 17862912 | 99.9% |
Reaction Steps
A solution of 0.21 g (5.5 mmoles) of lithium aluminum hydride dissolved in 70 ml of THF was cooled to −30° C. Thereto was gradually added a solution of 3 g (10.9 mmoles) of 5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde dissolved in 30 ml of tetrahydrofuran. The resulting mixture was stirred at −30° C. for 30 minutes to give rise to a reaction. After the completion of the reaction, ethyl acetate was added, followed by stirring. Then, water was added, followed by stirring for a while. The reaction mixture was filtered under vacuum. The filtrate was extracted 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 3.0 g (yield: 99.9%) of (5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07833939B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-11edac7a272d405db4a49225362489b9 |
|---|
| Source note | uspto-grants-2010_11 |
|---|