HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690151Generated: November 2, 2026
Triphenylphosphine → HCID 59201006, compound
https://huagongshe.com/reaction/1690151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-methyl-5-[4-(propan-2-yloxy)phenyl]imidazolidine-2,4-dione | HCID 3052153 | — |
| Reactant | HCID 59200893 | HCID 59200893 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Diethyl azodicarboxylate | HCID 5462977 | — |
| Product | HCID 59201006 | HCID 59201006 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153634B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-a1e0785b81da402d8d41535baae977c1 |
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| Source note | uspto-grants-2012_04 |
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