HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-(1-Benzylpiperidin-2-yl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Piperidin-2-ylethanol | HCID 15144 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(1-Benzylpiperidin-2-yl)ethan-1-ol | HCID 10242551 | — |
Reaction Steps
To a stirred solution of piperidine-2-ethanol (20 g, 155 mmol) in ethanol (240 mL) was added K2CO3 (106 g, 775.1 mmol) followed by addition of benzyl bromide (18.4 mL, 155.04 mmol) at 0° C. The reaction mixture was stirred at rt overnight, filtered through a sintered funnel and concentrated. The crude material was dissolved in ethyl acetate, the organic layer was washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated to get liquid compound 49.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08865741B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-8d761a23fb7743ddb3bb6b93c5fa14c2 |
| Source note | uspto-grants-2014_10 |