HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → cis-4-Azidomethyl-1-tert-butoxycarbonyl-3-methoxypiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | cis-4-Azidomethyl-1-tert-butoxycarbonyl-3-hydroxypiperidine | HCID 86657830 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | cis-4-Azidomethyl-1-tert-butoxycarbonyl-3-methoxypiperidine | HCID 86753637 | — |
Reaction Steps
To a solution of 60% sodium hydride (0.58 g) in dimethylformamide (10 ml) was added dropwise a solution of cis-4-azidomethyl-1-tert-butoxycarbonyl-3-hydroxypiperidine (3.4 g) in dimethylformamide (50 ml), and the resulting mixture was stirred at room temperature for 1 hr. Methyl iodide (1.24 ml) was added to the mixture with stirring, and the resulting mixture was stirred at room temperature for 15 hr. Water was added to the reaction mixture and the mixture was extracted with chloroform. The organic layer was washed with brine and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform) to give 1.5 g of cis-4-azidomethyl-1-tert-butoxycarbonyl-3-methoxypiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05864039 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-c09afe9b25b3429698b8d2d347524c88 |
| Source note | uspto-grants-1999_01 |