HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 5-(1-Azido-2-ethylbutyl)-1-(benzyloxy)-1H-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 1-[1-(Benzyloxy)-1H-pyrazol-5-yl]-2-ethylbutan-1-ol | HCID 68593374 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(1-Azido-2-ethylbutyl)-1-(benzyloxy)-1H-pyrazole | HCID 86600008 | 67.2% |
Reaction Steps
To a stirred mixture of 1-[1-(benzyloxy)-1H-pyrazol-5-yl]-2-ethylbutan-1-ol (0.492 g, 1.79 mmol) in THF (17 mL) at 0° C. under a nitrogen atmosphere was added triphenyl phosphine (0.705 g, 2.69 mmol) followed by diethyl azodicarboxylate (0.42 mL, 2.7 mmol). Diphenyl phosphoryl azide (0.58 mL, 2.7 mmol) was then added over 4 min. The mixture was allowed to attain ambient temperature and stirred for 16 h. The solvent was then evaporated in vacuo producing a crude oil which was purified on a Biotage column (hexane/ethyl acetate, 9:1). This afforded the product as a clear colorless oil (0.36 g, 67%). Mass Spectrum (+ESI): 300 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07399778B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-340f8ebbb9db438f82975011bd07a093 |
| Source note | uspto-grants-2008_07 |