HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2-Acetoxyethyl)-1-tert-butoxycarbonylpiperidine → 4-(2-Acetoxyethyl)-1-tert-butoxycarbonylpiperidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2-Acetoxyethyl)-1-tert-butoxycarbonylpiperidine | HCID 21840016 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Catalyst | Ruthenium tetroxide | HCID 119079 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2-Acetoxyethyl)-1-tert-butoxycarbonylpiperidin-2-one | HCID 21840025 | — |
Reaction Steps
The product from Step B (0.275 g, 1.01 mmol) was dissolved in ethyl acetate (5 mL). A solution of sodium periodate in water (0.5 g in 5 mL) and ruthenium tetroxide (13 mg, 0.10 mmol) was added, and the heterogeneous reaction stirred vigorously overnight at room temperature. An additional portion of sodium periodate in water was added (0.5 g in 5 mL) and the reaction stirred overnight. The reaction was quenched with 10% sodium thiosulfate, and filtered through celite. The phases were separated, and the organic phase dried over magnesium sulfate. Filtration and evaporation gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05965578 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-e9f33ce16e3a4a5a9567fa8dacac5ba3 |
| Source note | uspto-grants-1999_10 |