HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391802Generated: November 1, 2026
Triphenylphosphine → HCID 58629900, compound
https://huagongshe.com/reaction/1391802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | Ethyl (4-hydroxy-2-methylphenoxy)acetate | HCID 21986458 | — |
| Reactant | HCID 58629869 | HCID 58629869 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58629900 | HCID 58629900 | 62% |
Reaction Steps
A stirred mixture of ethyl [(4-hydroxy-2-methylphenyl)oxy]acetate (664 mg, 3.16 mmol), 4-{6-[(1R)-2-(ethyloxy)-1-hydroxyethyl]-2-pyridinyl}benzonitrile (719 mg, 2.68 mmol) and triphenylphosphine (857 mg, 3.27 mmol) in dry DCM (35 mL) was cooled to 0° C. under nitrogen. DIAD (633 μL, 3.21 mmol) was added dropwise over 10 min, and the reaction mixture stirred at 0° C. for a further 2 h. DCM (120 mL) was added to the reaction mixture, washed with aq 1M NaOH (50 mL) and water (100 mL), dried (Na2SO4) and evaporated to give a yellow oil. Purification by Biotage™ chromatography (silica, 90 g cartridge) eluting with cyclohexane:EtOAc (8:1) afforded the title compound as a colourless oil (765 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07338960B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-c9e8b855c685469893a2cded33eadedf |
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| Source note | uspto-grants-2008_03 |
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