HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 68532581, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Piperidin-4-yl)propanoic acid--hydrogen chloride (1/1) | HCID 21198547 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 68532581 | HCID 68532581 | — |
Reaction Steps
A suspension of (piperidin-4-yl)ethylcarboxylate hydrochloride (8.6 g, 44.4 mmol) and K2CO3 (24.5 g, 0.17 mol) in acetone (200 ml) was added benzylbromide (9.11 g, 53.3 mmol) and heated to reflux for 12 h. The solvent was evaporated in vacuo and the residue added H2O (200 ml). The aqueous layer was extracted with Et2O (3×100 ml) and the organic extracts dried over Na2SO4, filtered and evaporated in vacuo. The residue was dissolved in acetone and HCl bubbled into the solution to give the hydrochloride precipitate. The precipitate was filtered, dried and recrystallized from acetone to give the expected product as a white solid (11.03 g, 87.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07834010B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-994eb27cb7044999b23d79a67bb2cc37 |
| Source note | uspto-grants-2010_11 |