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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039692Generated: October 31, 2026

Triethyl Phosphate → HCID 58266260, compound

https://huagongshe.com/reaction/2039692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl PhosphateHCID 6535—
ReactantEthyl AcetoacetateHCID 8868—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantHCID 58266265HCID 58266265—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58266260HCID 58266260—

Reaction Steps

The reaction was carried out under argon. In succession, 4-formylbenzonitrile (656 mg, 5.0 mmol), 1-[4-fluoro-3-(trifluoromethyl)phenyl]urea (1.11 g, 5.0 mmol) and ethyl acetoacetate (651 mg, 5.0 mmol) were added to a solution of ethyl polyphosphate (2.0 g; prepared from triethyl phosphate and diphosphorus pentoxide analogously to the process in Example 18A) in THF (25 ml). The mixture was stirred under reflux for 19 h and then concentrated. Ethyl acetate (150 ml) was added to the residue, and the mixture was washed successively with water (50 ml), saturated sodium bicarbonate solution (50 ml) and saturated sodium chloride solution (50 ml). The organic phase was dried over sodium sulphate and concentrated. The residue was purified by silica gel chromatography (mobile phase: cyclohexane→cyclohexane/ethyl acetate 2:3). This gave 1.40 g (63% of theory) of the target product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580800B2
Source datasetuspto-grants-2013_11
ORD IDord-5f34a0f8d8b9492c85cb5dbabe8f661b
Source noteuspto-grants-2013_11