HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 178471300, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 18624169 | HCID 18624169 | — |
| Reactant | HCID 178526251 | HCID 178526251 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178471300 | HCID 178471300 | — |
Reaction Steps
A solution of diethyl azodicarboxylate (157 mg, 0.9 mmol) in 2 ml THF was added to a solution of the product of STEP 7 (197 mg, 0.66 mmol) and triphenylphosphine (236 mg, 0.9 mmol) in 5 ml THF at room temperature and stirred for 15 min. 2-(3-Hydroxypropylamino)pyridine N-oxide (168 mg, 0.9 mmol) was added. The reaction was stirred at room temperature for 18 h. THF was evaporated and the residue was purified by chromatography (on silica gel, CH2Cl2/CH3OH/NH4OH-98.5/1/0.5) to afford a clean product in 154 mg. NMR spectra of the product were consistent for the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06531494B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-440aae1b4d8f4dd492fe228cfd14d8b3 |
| Source note | uspto-grants-2003_03 |