HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl isocyanate → HCID 54382464, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 18734916 | HCID 18734916 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Nitroethane | HCID 6587 | — |
| Product | HCID 54382464 | HCID 54382464 | — |
Reaction Steps
A solution of phenylisocyanate (0.93 ml) in benzene (5 ml) was added to a mixture of 1-tert-butyldimethylsilyl-4(S)-ethynyl-2-azetidinone (1.0 g) in benzene (10 ml), nitroethane (0.35 ml), and triethylamine (0.1 ml) in benzene (5 ml) at room temperature. The reaction mixture was refluxed for 8 hours, then evaporated in vacuo. The residue was purified by column chromatography on silica gel eluting with n-hexane-ethyl acetate (9:1) to give 1-tert-butyldimethylsilyl-4(S)-(3-methyl-5-isoxazolyl)-2-azetidinone (0.96 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06384028B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-4b1b7613e18146ad923babdea79490c8 |
| Source note | uspto-grants-2002_05 |