HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Iodopentane → 1-(4-Nitrophenyl)-3-n-pentyl-3-azabicyclo[3.1.1]heptane-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Iodopentane | HCID 12335 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione | HCID 14872629 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Nitrophenyl)-3-n-pentyl-3-azabicyclo[3.1.1]heptane-2,4-dione | HCID 14872631 | — |
Reaction Steps
0.36 g of sodium hydride is added to a solution of 2.46 g of 1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione in 25 ml of N,N-dimethylformamide and the whole is stirred at room temperature for 30 minutes. 2.96 g of n-pentyl iodide dissolved in 10 ml of N,N-dimethylformamide are then added dropwise thereto. When the reaction is complete, the reaction mixture is freed of N,N-dimethylformamide. The residue is partitioned between ethyl acetate and water, and the organic phase is dried over magnesium sulphate and, after concentration by evaporation, the product is obtained having a melting point of 75°-79°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04764640 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-1b55430b595f47a39e2c835ea686551d |
| Source note | uspto-grants-1988_08 |