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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662026Generated: October 30, 2026

Water → HCID 66767035, compound

https://huagongshe.com/reaction/1662026

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 numberUS08030302B2
Source datasetuspto-grants-2011_10
ORD IDord-a8ee29b7c8f544d0b3c51f4d2a1a8501
Source noteuspto-grants-2011_10