HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (1-Ethylpiperidin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidin-3-ylmethanol | HCID 107308 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1-Ethylpiperidin-3-yl)methanol | HCID 20439432 | — |
Reaction Steps
To a stirring mixture of 3-piperidinemethanol (2 g) and potassium carbonate (6 g) in dry N,N-dimethylformamide (15 ml) was added iodoethane (1.53 ml). The reaction became warm and was cooled back to ambient temperature using a cold water bath. After 2 hours, the solvent was stripped, the residue treated with water and extracted three times with ethyl acetate. The combined extracts were washed with water then brine, dried by passing through a phase separation cartridge and evaporated to give the title compound as a clear oil, yield 1.53 g, 61%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563717B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-aad8f65478624ae2baf9001d9ecb5a20 |
| Source note | uspto-grants-2013_10 |