HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Methyl 3-(2-oxopiperidin-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3-(5-bromopentanoylamino)benzoate | HCID 10686692 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-(2-oxopiperidin-1-yl)benzoate | HCID 10681135 | 56.2% |
Reaction Steps
The bromide of Example 36 (1.50 g, 4.88 mmol) was taken up in dry DMF (40 ml) and treated with NaH (160 mg, 80% disp. in oil) at 0° C. The mixture was stirred at r.t. under nitrogen for 10 min, then KI (80 mg) added and the mixture heated at 70° C. for 4 h. The mixture was evaporated and partitioned between EtOAc and 1M HCl. The organic portion was washed with 5% KHCO3 and brine, filtered (Whatman® 1 PS, phase separator) and evaporated. The residue was chromatographed (eluant 2% MeOH in EtOAc) to provide a colourless oil (640 mg, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728829 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-39e2a12366cc4afaa1054c2e96602afd |
| Source note | uspto-grants-1998_03 |