HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726980Generated: November 1, 2026
Triphenylphosphine → HCID 69036617, compound
https://huagongshe.com/reaction/1726980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | 2-[2-Methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-ethanol | HCID 21935831 | — |
| Reactant | HCID 69039165 | HCID 69039165 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69036617 | HCID 69036617 | — |
Reaction Steps
0.26 g (1.0 mmol) of the above prepared [rac]-3-(4-hydroxy-naphthalen-2-yl)-2-methoxy-propionic acid methyl ester, 0.30 g (1.05 mmol) of 2-[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-ethanol (see below example 4K]) and 0.31 g (1.20 mmol) of triphenylphosphine were dissolved in 10 ml of THF. The stirred reaction mixture was cooled down to 0° C. and a solution of 0.27 g (1.15 mmol) of di-tert.-butyl azodicarboxylate in 5 ml of THF was added drop by drop and the reaction warmed up to ambient temperature. After 20 hours, the solvent was evaporated and the residue purified by chromatography (SiO2, heptane/EtOAc=9:1 to 1:1) to give 0.45 g of the title compound as light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07495001B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-5513061e4d884e3095b27081b8e49625 |
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| Source note | uspto-grants-2009_02 |
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