HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 1-Boc-4-(2-pyridyloxy)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | HCID 178516071 | HCID 178516071 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Boc-4-(2-pyridyloxy)piperidine | HCID 21906039 | — |
Reaction Steps
To a solution of 2-hydroxypyridine (2.0 g), tert-butyl 4-hydroxy-1-piperidinecarboxylate (5.3 g) and triphenylphosphine (8.3 g) in tetrahydrofuran (63 ml) was slowly added diethyl azodicarboxylate (5.5 g) at 8° C., and the mixture was stirred at room temperature for 4 hours. The reaction mixture was concentrated in vacuo to give the crude product of the title compound and the crude product was purified by chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129243B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-c8d9c4749fb54a3599bbfd5cec6c6a38 |
| Source note | uspto-grants-2006_10 |