HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → HCID 18473723, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Piperidin-2-ylethanol | HCID 15144 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18473723 | HCID 18473723 | 40% |
Reaction Steps
A! A solution of 1N sodium hydroxide (156 ml, 0.156 mole) was added to a mixture of 2-piperidine-ethanol (20 ml, 0.156 mole) and butyl bromide (21 ml, 0.187 mole) in ethanol (200 ml). The reaction mixture was refluxed for 4 hours, then the solvent was evaporated under vacuum. The aqueous solution was acidified with HCl and washed with ethyl ether, then it was treated with a 32% solution of sodium hydroxide until pH-12 and extracted with ethyl ether. The combined organic phases were anhydrified over sodium sulfate and the solvent was evaporated under vacuum. The resulting crude was purified by distillation yielding 1.7 g of N-butyl-2-piperidine-ethanol (b.p.: 88°-99° C./0mmHg) (yield: 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05827881 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-ad793f1392ec4814b457edd404b3012a |
| Source note | uspto-grants-1998_10 |