HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598731Generated: October 26, 2026
Tetrahydrofuran → (5-Tert-butyl-2-p-tolyl-2h-pyrazol-3-yl)-methanol
https://huagongshe.com/reaction/598731
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 5-tert-Butyl-2-p-tolyl-2H-pyrazole-3-carboxylic acid ethyl ester | HCID 57418554 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (5-Tert-butyl-2-p-tolyl-2h-pyrazol-3-yl)-methanol | HCID 67091382 | 96% |
Reaction Steps
To an oven dried round bottom flask containing 5-tert-Butyl-2-p-tolyl-2H-pyrazole-3-carboxylic acid ethyl ester (0.64 g, 2.2 mmol) was added anhydrous THF (20 mL) followed by the drop wise addition of DIBAL-H (0.96 mL, 4.9 mmol) under nitrogen. After stirring at room temperature for 30 minutes the reaction was diluted with 100 mL diethyl ether and quenched with 5 mL Methanol stirring for an additional 30 minutes at room temperature. The resulting slurry was treated with 5 g MgSO4 and filtered through a pad of diatomaceous earth. The filter cake was washed with 3×75 mL portions of ether and the combined filtrates concentrated under vacuo to afford the desired alcohol as a clear oil (0.515 g, 96%). No further purification was necessary. Expected mass=244. Observed mass=245.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897599B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-13bea3c0a3e74346840fd7a718ac250e |
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| Source note | uspto-grants-2011_03 |
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