HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,2,2-Trifluoro-1-(3-hydroxypiperidin-1-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 3-Hydroxypiperidine | HCID 23293 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,2,2-Trifluoro-1-(3-hydroxypiperidin-1-yl)ethanone | HCID 58992584 | 85.2% |
Reaction Steps
Ethyl trifluoroacetate (1.31 mL, 11.0 mmol) and triethylamine (1.68 mL, 12.0 mmol) were added to 3-hydroxypiperidine (1.01 g, 10.0 mmol) in ethanol (10 mL). The mixture was stirred at room temperature for 8 hours. Subsequently, the reaction mixture was concentrated and water was added. The mixture was then extracted with ethyl acetate and the extract washed with brine and dried over magnesium sulfate. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=10:1->2:1) gave 1.68 g (85%) of the desired compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902367B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-b402d2792c5e4687b940034055329816 |
| Source note | uspto-grants-2011_03 |