HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzyl 2-(4-oxopiperidin-1-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Piperidone | HCID 33721 | — |
| Reactant | HCID 9991399 | HCID 9991399 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Benzyl 2-(4-oxopiperidin-1-yl)acetate | HCID 18187989 | 83% |
Reaction Steps
To a stirred suspension of 4-piperidone (10.0 g, 65.0 mmol) and bromobenzyl acetate (14.9 g, 65.2 mmol) in acetone (100 ml) was added K2CO3 (9.0 g) and Et3N (9.1 ml, 65.2 mmol). The reaction mixture was stirred at room temperature for two days, and then the solvent was evaporated. The residue was partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc. The organic extracts were combined and dried over Na2SO4. The solvent was evaporated to afford the title compound (13.3 g, 53.8 mmol, 83%) as a thick oil. 1H NMR (300 MHz, CDCl3) δ 7.33-7.37 (m, 5H), 5.18 (s, 2H), 3.42 (s, 2H), 2.91 (t, J=6.1 Hz, 4H), 2.50 (t, J=6.1 Hz, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297260B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-935551db6865440b9ffada4c72ee8ce8 |
| Source note | uspto-grants-2001_10 |