HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499603Generated: November 2, 2026
Triphenylphosphine → HCID 86726822, compound
https://huagongshe.com/reaction/1499603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diphenylphosphoryl azide | HCID 123414 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 86726819 | HCID 86726819 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86726822 | HCID 86726822 | 86.5% |
Reaction Steps
To a solution of tert-butyl (4R)-4-((1R,2S)-1-{[tert-butyl(dimethyl)silyl]oxy}-2-cyclopropyl-3-hydroxypropyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (1.3 g, 3.0 mmol) and triphenylphosphine (1.6 g, 6.1 mmol) in anhydrous THF (20 mL), DIAD (1.2 mL, 5.9 mmol) was added drop-wise under an atmosphere of nitrogen. Upon completion of addition, a precipitate was formed. The reaction mixture was stirred for 30 min. then diphenylphosphonic azide (1.3 mL, 6.2 mmol) in anhydrous THF (1.0 mL) was added. After stirring at ambient temperature for 3 h, the volatile organic solvents were removed under reduced pressure and the crude product was purified by flash column chromatography (120 g of silica gel, eluting with 0-15% EtOAc-hexanes) to afford the sub-title compound as a light yellow oil (1.18 g, 86%). LC/MS (ESI) m/z calc. for C17H35N4O2Si: 355.30 [M-Boc+H]+. found: 355.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200004B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-bf3dc55b43e7447fa655cef86f6b0b9a |
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| Source note | uspto-grants-2015_12 |
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