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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369831Generated: October 31, 2026

Hydrazine hydrate (1:1) → HCID 135508237, compound

https://huagongshe.com/reaction/2369831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 59028462HCID 59028462—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 135508237HCID 13550823711%

Reaction Conditions

Temperature382.5 °C

Reaction Steps

To a mixture of (4E)-1-(6-hydroxy-1-benzofuran-2-yl)-5-phenylpent-4-ene-1,3-dione (0.48 mmol) and hydrazine monohydrate (0.02 g, 0.48 mmol) were added ethanol (24 mL) and acetic acid (1 drop) in a sealed tube. The reaction was heated at 65-700° C. overnight. The solvent was removed under reduced pressure to afford crude product. The crude product was purified by reverse phase HPLC. The fractions from HPLC were combined, neutralized with 1.0 N aqueous sodium hydroxide solution, and diluted with ethyl acetate (200 mL). The organic layer was washed with saturated aqueous sodium chloride (50 mL), dried over magnesium sulfate, filtered, and concentrated to afford the product (11% yield): 1H NMR (400 MHz, CD3Cl): δ 7.58 (br d, 2H), 7.35 (m, 4H), 7.25 (t, 2H), 7.10 (br d, 1H), 7.05 (br s, 1H), 6.94 (br d, 1H), 6.88 (br s, 1H), 6.75 (dd, 1H); MS (EI) for C19H14N2O2: 303 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710038B2
Source datasetuspto-grants-2014_04
ORD IDord-7bbf47c5a6664d69a9c4302ca29e6e87
Source noteuspto-grants-2014_04