HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967478Generated: October 31, 2026
Triphenylphosphine → HCID 69652272, compound
https://huagongshe.com/reaction/967478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,4-Dichlorophenethyl alcohol | HCID 2734099 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | HCID 69652311 | HCID 69652311 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69652272 | HCID 69652272 | — |
Reaction Steps
410 mg (1.95 mmol) of 7-Hydroxy-benzo[1,3]dioxole-5-carboxylic acid ethyl ester was dissolved in 20 ml of anhydrous tetrahydrofuran. To this solution was added 410 mg (2.15 mmol) of 2-(2,4-Dichlorophenyl)-ethanol, 1.9 g (equivalent to 5.85 mmol PPh3) of triphenylphosphine derivatized polystyrene and 1.0 g (5.85 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 | US06953857B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-e2754ded637a4f09b7f52d53317293d9 |
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| Source note | uspto-grants-2005_10 |
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