HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride → HCID 178463888, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride | HCID 2723880 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Diethyl guanidinium trifluoroacetate | HCID 131731834 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178463888 | HCID 178463888 | 70% |
Reaction Steps
To a solution of 1-benzyl-3-oxo-piperidine-4-carboxylic acid ethyl ester hydrochloride (2.11 g, 7.1 mmol) in EtOH (35 mL) was added diethyl guanidinium trifluoroacetate (1.5 g, 7.1 mmol) and sodium ethoxide (21 wt % in EtOH, 6.7 mL). The reaction was heated at reflux for 16 h then cooled to room temperature (rt). The reaction mixture was diluted with H2O and extracted with CH2Cl2 (2×). The combined organic extracts were dried and concentrated. The resulting material was triturated with Et2O to give the title compound (1.54 g, 70%) as a light brown solid. MS (ESI): mass calcd. for C18H24N4O, 312.4; m/z found, 313.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829011B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-01d0cbeaf12b453bb38a50e5542cd9ac |
| Source note | uspto-grants-2014_09 |