HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 18665572, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | tert-Butyl (((1,1-dimethylethoxy)carbonyl)oxy)carbamate | HCID 2728863 | — |
| Reactant | HCID 18665558 | HCID 18665558 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18665572 | HCID 18665572 | 67% |
Reaction Steps
To a mixture of 3-[3-(4,5-dihydro-4(R)-phenyloxazol-2-yl)-2-fluorophenyl]-2-propyn-1-ol (1.41 g, 4.8 mmol), N,O-bis(tert-butoxycarbonyl)hydroxylamine (1.11 g, 4.8 mmol) and triphenylphosphine (1.63 g, 6.2 mmol) in dry tetrahydrofuran (350 ml) was added dropwise a solution of diethyl azodicarboxylate (1.08 g, 6.2 mmol) in dry tetrahydrofuran (15 ml). The reaction mixture was stirred for 2 hours and volatiles removed by evaporation. The residue was purified by column chromatography on silica gel eluting with ethyl acetate-hexane (=1:10) to afford N,O-di(tert-butoxycarbonyl)-[3-[3-(4,5-dihydro-4(R)-phenyloxazol-2-yl)-2-fluoro-phenyl]-2-propyn-1-yl]hydroxylamine (1.64 g, 67%) as pale yellow plates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05814648 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-60763c2a998846a390f722b694a7b841 |
| Source note | uspto-grants-1998_09 |