HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → tert-Butyl 3-methoxy-4-oxopiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | 1-Boc-3,4,4-trimethoxypiperidine | HCID 59263089 | — |
| Solvent | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | tert-Butyl 3-methoxy-4-oxopiperidine-1-carboxylate | HCID 57363786 | — |
Reaction Steps
To a solution of 1,1-dimethylethyl 3,4,4-tris(methyloxy)-1-piperidinecarboxylate D17 (4.85 g) in HCl/1,4-Dioxane (50 mL) was heated at 50° C. and stirred overnight. Water (50 ml) was added to the reaction mixture and the pH adjusted to 10.0 using sodium hydroxide. After that BOC anhydride (4.22 g, 19.4 mmol) was added to the reaction mixture and stirred for 4 hours. The resulting mixture was extracted with EtOAc (3×100 ml). The organic layer was dried over anhydrous MgSO4, concentrated in vacuo to afford the desired product D18 in 3.1 g. LCMS [M-55][email protected] min (5 min run)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045485B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-545840e34cca4f5fb63f3a87db2506a7 |
| Source note | uspto-grants-2015_06 |