HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (1-benzyl-1H-pyrazol-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 1-benzyl-1H-pyrazole-4-carboxylate | HCID 45073393 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-benzyl-1H-pyrazol-4-yl)methanol | HCID 16769828 | 98.2% |
Reaction Steps
In a nitrogen atmosphere, 1.44 g of lithium aluminum hydride was added to 100 ml of tetrahydrofuran, and a solution of 7.39 g of methyl 1-benzyl-1H-pyrazole-4-carboxylate in 50 ml of tetrahydrofuran was added dropwise at 0° C. over 30 minutes. Thereafter, the mixture was stirred at room temperature for 5 hours. The reaction mixture was cooled to 0° C., and 15 ml of a 1 mol/L aqueous potassium hydroxide solution was added dropwise. Precipitates were filtered, washed with tetrahydrofuran and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 6.32 g of (1-benzyl-1H-pyrazol-4-yl)methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846956B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-9df0a5f6958b4546af460d0b06b562dd |
| Source note | uspto-grants-2010_12 |