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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium sodium tartarateHCID 9855836—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantEthyl 5-Bromo-1-methyl-1H-pyrazole-4-carboxylateHCID 53302113—
SolventTetrahydrofuranHCID 8028—
Product(5-bromo-1-methyl-1H-pyrazol-4-yl)methanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829010B2
Source datasetuspto-grants-2014_09
ORD IDord-05bc563ebc814784873be429d31ae7f8
Source noteuspto-grants-2014_09