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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588272Generated: October 29, 2026

Sulfuric Acid → 5-(1-phenyl-1H-pyrazol-5-yl)indolin-2-one

https://huagongshe.com/reaction/588272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPhenylhydrazineHCID 7516—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 90417345HCID 90417345—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-(1-phenyl-1H-pyrazol-5-yl)indolin-2-oneHCID 9041780142.1%

Reaction Steps

To a solution of 5-(3,3-diethoxyprop-1-ynyl)indolin-2-one (100 mg, 0.39 mmol) in acetonitrile (5 ml) were added phenyl hydrazine (38 μL, 0.38 mmol) and sulfuric acid (52 μL, 0.98 mmol), and the mixture was stirred for 3 h at room temperature, then the mixture was stirred for 2 h at 50° C. The reaction mixture was poured into water (50 mL), and the resulting precipitate was filtered and dried. The precipitated was dissolved in acetonitrile (5 mL), then water (52 μL, 3.9 mmol) and sulfuric acid (93 μL, 1.75 mmol) were added. The mixture was heated at 80 C for 4 h. The mixture was cooled to room temperature, and then neutralized with sat. NaHCO3. The mixture was extracted with CHCl3/EtOAc 3 times. The combined organic extracts were washed with sat. NaCl, dried over Na2SO4, and evaporated in vacuo. The residue purified by column chromatography (EtOAc/n-hexane) to give the title compound as a brown solid (44 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227962B2
Source datasetuspto-grants-2016_01
ORD IDord-789a5e75e1a8482cb753c94eb7d01643
Source noteuspto-grants-2016_01