HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 19390903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19390924 | HCID 19390924 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19390903 | HCID 19390903 | — |
Reaction Steps
In 30 ml of ethanol was dissolved 3.13 g of the 1-acetyl-4-[4-(ethylamino)benzyl]piperidine (Compound No. 8) prepared in Example 16, followed by addition of 3.31 g of potassium carbonate and 1.43 ml of benzyl bromide. The mixture was refluxed for 2 hours and the insolubles were filtered off. The solvent was then distilled off and the remaining oil was purified by silica gel column chromatography (eluent: ethyl acetate) to give 3.8 g of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441967 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-6f712bcbe33c4a4080ee2271f2070f27 |
| Source note | uspto-grants-1995_08 |