HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72721Generated: October 29, 2026
Potassium sodium tartarate → (5-bromo-1-methyl-1H-pyrazol-4-yl)methanol
https://huagongshe.com/reaction/72721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Ethyl 5-Bromo-1-methyl-1H-pyrazole-4-carboxylate | HCID 53302113 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-bromo-1-methyl-1H-pyrazol-4-yl)methanol | HCID 84662962 | — |
Reaction Steps
A solution of ethyl 5-bromo-1-methyl-1H-pyrazole-4-carboxylate (2.00 g, 8.58 mmol) in tetrahydrofuran (30 mL) at 0° C. was treated with diisobutylaluminum hydride (1 M solution in tetrahydrofuran, 18.9 mL, 18.9 mmol), and the mixture was allowed to warm to room temperature and stir for 18 hours. Saturated aqueous sodium potassium tartrate solution was added, and stirring was continued for 4 hours. The aqueous layer was extracted with ethyl acetate, and the combined organic layers were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. Purification via silica gel chromatography (Eluent: 100:1 ethyl acetate/methanol) afforded the product. Yield: 1.63 g, 8.53 mmol, 99%. LCMS m/z 192.9 (M+1). 1H NMR (400 MHz, CDCl3) δ 2.44 (s, 1H), 3.84 (s, 3H), 4.48 (s, 2H), 7.51 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829010B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-05bc563ebc814784873be429d31ae7f8 |
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| Source note | uspto-grants-2014_09 |
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