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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68692Generated: October 27, 2026

Potassium Carbonate → 6-bromo-3-ethyl-1-phenyl-1H-indazole

https://huagongshe.com/reaction/68692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86658768HCID 86658768—
Reactant(E)-1-(1-(4-bromo-2-fluorophenyl)propylidene)-2-phenylhydrazineHCID 86658769—
SolventDimethylformamideHCID 6228—
Product6-bromo-3-ethyl-1-phenyl-1H-indazoleHCID 67449468—

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a 1000-mL 3-necked round-bottom flask, was placed a solution of (Z)-1-(1-(4-bromo-2-fluorophenyl)propylidene)-2-phenylhydrazine and (E)-1-(1-(4-bromo-2-fluorophenyl)propylidene)-2-phenylhydrazine (44.3 g, 138.01 mmol, 1.00 equiv) in N,N-dimethylformamide (400 mL), potassium carbonate (83 g, 601.45 mmol, 4.40 equiv). The resulting solution was stirred for 2 days at 100° C. in an oil bath. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with water (500 mL). The resulting solution was extracted with ethyl acetate (2×300 mL) and the organic layers combined. The resulting mixture was washed with water (2×300 mL) and brine (1×300 mL). The resulting mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:50) to yield 6-bromo-3-ethyl-1-phenyl-1H-indazole as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822447B2
Source datasetuspto-grants-2014_09
ORD IDord-abdf7059708c4ed3933b2679f4cff480
Source noteuspto-grants-2014_09