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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639764Generated: October 26, 2026

Propargyl alcohol → 3-(2-methyl-2H-indazol-4-yl)prop-2-yn-1-ol

https://huagongshe.com/reaction/1639764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant4-Bromo-2-methyl-2H-indazoleHCID 22559031—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product3-(2-methyl-2H-indazol-4-yl)prop-2-yn-1-olHCID 5933464546%

Reaction Conditions

Temperature70 °C

Reaction Steps

Under argon gas atmosphere, a mixture of 4-bromo-2-methyl-2H-indazole (1.00 g, 4.74 mmol), propargyl alcohol (1.10 mL, 18.9 mmol) and bis(triphenylphosphine)palladium(II) dichloride (665 mg, 0.947 mmol) in triethylamine (47 mL) was stirred at 70° C. for 14 hr, and concentrated under reduced pressure. The residue was dissolved in ethyl acetate, and insoluble material was filtered off. The filtrate was washed with water and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane=70/30→100/0) and the obtained crudely purified product was washed with ethyl acetate to give the title compound (403 mg, yield 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110585B2
Source datasetuspto-grants-2012_02
ORD IDord-7ea6a80475464285ac61c79dbf2a12ea
Source noteuspto-grants-2012_02