HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 11961748, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 22661867 | HCID 22661867 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11961748 | HCID 11961748 | 69% |
Reaction Steps
Triphenylphosphine (1.64 g, 6.24 mmol) was added to a solution of 2-benzyloxy-5-cyano-benzylazide (1.1 g, 4.16 mmol) in anhydrous THF (10 mL) at 0° C. After 1 hour, ammonium hydroxide (0.5 mL) was added and the mixture was warmed to room temperature and stirred overnight. The mixture was concentrated and the residue purified by flash chromatography (3% methanol/dichloromethane) to afford 677 mg (69%) of the title compound as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.6-7.3 (m, 7H); 6.95 (d, 1H, J=9.1 Hz); 5.18 (s, 2H); 3.9 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06803457B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-27140a9d3977445ca265dd4987084230 |
| Source note | uspto-grants-2004_10 |