HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948383Generated: October 30, 2026
Triphenylphosphine → HCID 131730338, compound
https://huagongshe.com/reaction/1948383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diphenylphosphoryl azide | HCID 123414 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 87481887 | HCID 87481887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131730338 | HCID 131730338 | 71.4% |
Reaction Steps
In a flame-dried flask triphenylphosphine (3.86 g; 14.7 mmol; 2 eq.) was dissolved in anhydrous THF (15 ml) and cooled to 0 C. DIAD (2.97 g; 14.7 mmol; 2 eq.) was slowly added dropwise. Upon addition a white precipitate formed. A THF solution containing tert-butyl-4-[(diphenylmethylene)amino]-3-hydroxypiperidine-1-carboxylate (Intermediate 268, 2.8 g; 7.36 mmol) was added (amount of THF added was such that the final concentration of alcohol was ca. 0.5-1M). The resultant reaction slurry was stirred at 0 C for 30 minutes. (PhO)2PON3 (4.05 g; 14.7 mmol; 2 eq.) was then added and the reaction was allowed to warm to RT and stirred for 12 hrs. Monitored by LC/MS. The reaction was concentrated and purified by flash column chromatography (0-30% EtOAc/hexanes with 0.1% triethylamine). Isolation gave 2.13 g of the title compound in 71% yield. LC/MS (ES+)[(M+H)+]: 406 for C23H27N5O2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399489B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d17308243e794bc2807c7b1cceccdf2e |
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| Source note | uspto-grants-2013_03 |
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