HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → (1-Ethylpiperidin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidin-3-ylmethanol | HCID 107308 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1-Ethylpiperidin-3-yl)methanol | HCID 20439432 | 99% |
Reaction Steps
To a solution of piperidin-3-ylmethanol (3.88 g) in dimethylformamide (50 mL) was added potassium carbonate (9.3 g) and ethyl bromide (2.52 mL). The reaction was stirred overnight at room temperature. The mixture was filtered and the filtrate evaporated. The residue was filtered through a short pad of silica eluting with 10% 7M NH3/MeOH in dichloromethane. The filtrate was evaporated to give the title compound as an orange oil (4.8 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07906645B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-a6a42df75e37456caa40517d23372d15 |
| Source note | uspto-grants-2011_03 |