HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-Benzyloxy-1-methoxy-pentane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-(Benzyloxy)pentan-1-ol | HCID 221194 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Benzyloxy-1-methoxy-pentane | HCID 22170556 | 70% |
Reaction Steps
1.6 g (0.039 mol) of 55% sodium hydride in oil were added to 50 ml of dimethylformamide under stirring at room temperature. 5 ml (0.026 mol) of 5-benzyloxy-1-pentanol and 2.43 ml (0.039 mol) of methyl iodide were then added successively. After a night the excess of sodium hydride was decomposed with water and the solvent evaporated under vacuum. The residue was redissolved with methylene chloride and washed with water. The organic layer was finally dried over anhydrous sodium sulfate and evaporated to give 3.5 g (70% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07037929B1 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-2f902dd068264514872be095c1a52f61 |
| Source note | uspto-grants-2006_05 |