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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517203Generated: October 31, 2026

Triethyl Phosphate → HCID 86732323, compound

https://huagongshe.com/reaction/517203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl PhosphateHCID 6535—
Reactant1,3-CyclohexanedioneHCID 10434—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant(3-Trifluoromethylphenyl)ureaHCID 25712—
Reactant4-Bromo-2-(methylsulfonyl)benzaldehydeHCID 2761076—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 86732323HCID 86732323—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of triethyl phosphate (400 μL, 428 mg, 2.35 mmol) and phosphorous pentoxide (216 mg, 1.52 mmol) is heated at 50° C. over night and dilutet with tert-butyl methyl ether (10 mL). Cyclohexane-1,3-dione (320 mg, 2.85 mmol), 4-bromo-2-(methylsulfonyl)benz-aldehyde (500 mg, 1.90 mmol) and 1-(3-(trifluoromethyl)phenyl)urea (388 mg, 1.90 mmol) are added, and the mixture is heated at reflux over night and concentrated under reduced pressure. The residue is purified by reversed phase HPLC (Agilent ZORBAX™+SB-C18, gradient of acetonitrile in water, 0.15% formic acid). Yield: 80 mg; ESI mass spectrum [(79Br)-M+H]+=543, [(81Br)-M+H]+=545, Retention time HPLC: 1.06 min (Z017_S04).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115093B2
Source datasetuspto-grants-2015_08
ORD IDord-29c65718670a4b0c90b1830e7991d2d7
Source noteuspto-grants-2015_08