HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 15946645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diphenylphosphoryl azide | HCID 123414 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 86636761 | HCID 86636761 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15946645 | HCID 15946645 | 86.3% |
Reaction Steps
DIAD (2.4 mL, 12.4 mmol) was added dropwise to a cooled (−5° C.) solution of Ph3P (3.1 g, 11.7 mmol) in THF (50 mL). After 30 min, a solution of 2 (5.57 g, 9.5 mmol) in THF (20 mL) was added. After an additional 10 min, diphenyl phosphorazidate (DPPA; 2.4 mL, 11.31 mmol) was added and the reaction mixture was allowed to attain rt. After stirring overnight, the solvent was evaporated and the residue was purified by silica gel chromatography to give 3 (5.0 g, 8.2 mmol, 86%) as a colorless oil. 13C-NMR (CDCl3) 138.17, 137.92, 137.38, 128.6-127.7, 78.2, 74.3, 73.9, 73.7, 73.5, 72.4, 69.5, 68.8, 62.2, 62.1, 62.0, 61.9, 61.0, 60.9, 27.9 (d, J=141 Hz), 16.5, 16.4; 31P-NMR (CDCl3) 27.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08062641B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-1614b4e9a8454057bc6fc749c07f89ea |
| Source note | uspto-grants-2011_11 |