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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195542Generated: November 2, 2026

Water → HCID 66767035, compound

https://huagongshe.com/reaction/2195542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(Triphenylphosphoranylidene)acetoneHCID 15038—
Reactant1,3-Diethyl 2-oxopropanedioateHCID 69105—
Reactant4-Fluorophenylhydrazine hydrochlorideHCID 69981—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 66767035HCID 6676703543.6%

Reaction Steps

To a suspension of 1-triphenylphosphoranylidene-2-propanone (3.18 g, 9.99 mmol) in THF (50 mL) is added diethyl ketomalonate (1.74 g, 9.99 mmol). The resulting mixture is stirred at RT for 30 min to give a clear solution. Then this solution is added to a solution of 4-fluorophenylhydrazine hydrochloride (1.62 g, 9.96 mmol) in EtOH:H2O (30 mL:30 mL). After the resulting mixture is refluxed for 1 hour, TEA (3 mL) is added and the mixture is stirred at reflux for another 1 hour. Then it is concentrated and the residue is partitioned with saturated aqueous NH4Cl (30 mL) and EtOAc (30 mL). The organic phase is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with PE:EtOAc (3:1) to give the product (1.20 g, 43% yield). MS (m/z): 277.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043878E1
Source datasetuspto-grants-2012_12
ORD IDord-0b45f11340ae4a75a1666a404d4ff25b
Source noteuspto-grants-2012_12