HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831809Generated: October 30, 2026
Triphenylphosphine → HCID 69652280, compound
https://huagongshe.com/reaction/1831809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,4-Dichlorophenethyl alcohol | HCID 2734099 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | HCID 69652274 | HCID 69652274 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69652280 | HCID 69652280 | — |
Reaction Steps
g (3.93 mmol) of 3,4-Diethoxy-5-hydroxy-benzoic acid ethyl ester was dissolved in 20 ml of anhydrous tetrahydrofuran. To this solution was added 0.83 g (4.33 mmol) of 2-(2,4-Dichlorophenyl)-ethanol, 3.93 g (equivalent to 11.8 mmol PPh3) of triphenylphosphine derivatized polystyrene and 2.05 g (11.8 mmol) of DEAD. The solution was shaken for 16 h at RT. The polymer was filtered off and washed with ethyl acetate. The solvent was removed under reduced pressure. The residue was taken-up in ethyl acetate and the solution was washed three times with water and twice with saturated aqueous sodium chloride. The organic phase was dried with magnesium sulphate, filtered and the solvent was removed under reduced pressure. The residue was chromatographed on silica gel eluting with ethyl acetate/n-heptane (1/5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067665B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-c6edef38356243519a23188403f7cb83 |
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| Source note | uspto-grants-2006_06 |
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