HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515076Generated: November 2, 2026
Triphenylphosphine → HCID 67058134, compound
https://huagongshe.com/reaction/1515076
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(Trifluoromethoxy)benzyl alcohol | HCID 142783 | — |
| Reactant | Diethylazodicarboxylate toluene | HCID 66777355 | — |
| Reactant | Ethyl 3-ethoxy-3-(4-hydroxyphenyl)propionate | HCID 67058135 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67058134 | HCID 67058134 | — |
Reaction Steps
Ethyl 3-ethoxy-3-(4-hydroxyphenyl)propionate (100 mg, 0.420 mmol) produced in Example 1 (1C) and 3-trifluoromethoxybenzyl alcohol (123 mg, 0.640 mmol) were dissolved in tetrahydrofuran (2 mL), and triphenylphosphine (165 mg, 0.629 mmol) and a diethyl azodicarboxylate toluene solution (2.2 M, 290 μL, 0.638 mmol) were added thereto at room temperature, and then, the resulting mixture was stirred under a nitrogen atmosphere at room temperature for 4 hours. The solvent in the reaction solution was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0 to 95:5 (v/v)), whereby the objective title compound was obtained as a colorless oily substance (124 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08222281B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-1e281d03fd4241069b4d084615b9f1af |
|---|
| Source note | uspto-grants-2012_07 |
|---|