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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690151Generated: November 2, 2026

Triphenylphosphine → HCID 59201006, compound

https://huagongshe.com/reaction/1690151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant5-methyl-5-[4-(propan-2-yloxy)phenyl]imidazolidine-2,4-dioneHCID 3052153—
ReactantHCID 59200893HCID 59200893—
SolventTetrahydrofuranHCID 8028—
SolventDiethyl azodicarboxylateHCID 5462977—
ProductHCID 59201006HCID 5920100666%

Reaction Steps

To a solution of 1-(3-(4-(1,1,1,3,3,3-hexafluoro-2-(methoxymethoxy)propan-2-yl)-2-propylphenoxy)phenyl) ethanol (40.0 mg, 85.8 mmol), 5-(4-(1-methylethoxy)phenyl)-5-methylimidazolidine-2,4-dione (32.0 mg) and triphenylphosphine (56.3 mg) in tetrahydrofuran (5 mL), diethylazodicarboxylate (about 2.2 mol/L toluene solution, 97.5 μL) was added under ice-cold conditions. After completion of the reaction, the reaction solution was concentrated in vacuo. The obtained residue was purified using silica-gel thin-layer chromatography (hexane/ethyl acetate). The obtained compound was added with 2 mol/L hydrogen chloride-ethyl acetate solution (1 mL) at room temperature. After completion of the reaction, the solution was concentrated in vacuo and purified using thin-layer silica-gel column chromatography (hexane/ethyl acetate) and the title compound (37.2 mg, yield 66%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153634B2
Source datasetuspto-grants-2012_04
ORD IDord-a1e0785b81da402d8d41535baae977c1
Source noteuspto-grants-2012_04