HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86641939, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-Bromo-5-hydroxypyridine | HCID 2762865 | — |
| Reactant | 2-Phenoxybenzyl alcohol | HCID 3660111 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86641939 | HCID 86641939 | — |
Reaction Steps
To a solution of 6-bromopyridin-3-ol (1.76 g) in tetrahydrofuran (20 ml), 3.20 g of triphenylphosphine, 5.52 ml of diethyl azodicarboxylate (45% toluene solution) and 2.43 g of (2-phenoxyphenyl)methanol were added, and the reaction solution was stirred overnight at room temperature. The reaction solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: ethyl acetate/hexane (0:100-15:85)) to afford the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367708B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-a6bb457da661413a8ea1867335fcd100 |
| Source note | uspto-grants-2013_02 |