HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 1-(2,2,2-trifluoroethyl)piperidin-4-ylcarbamate → 1-(2,2,2-Trifluoroethyl)piperidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 1-(2,2,2-trifluoroethyl)piperidin-4-ylcarbamate | HCID 22562166 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(2,2,2-Trifluoroethyl)piperidin-4-amine | HCID 16228722 | — |
Reaction Steps
[1-(2,2,2-Trifluoroethyl)piperidin-4-yl]-carbamic acid tert-butyl ester was then taken up in dioxane (80 mL) and hydrogen chloride gas was bubbled through the solution for 10 minutes. The reaction vessel was capped tightly and stirred for 1.5 hours. The solvent was removed under reduced pressure at 40° C. The residue was taken up in 42 mL of 0.5M sodium methoxide in methanol, stirred at room temperature for 3 hours, and filtered. The filtrate was concentrated, taken up in ethyl acetate, filtered, and concentrated to give 1.0 g of 1-(2,2,2-trifluoroethyl)piperidin-4-ylamine as a dark colored oil, (M+H)+=183.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451804B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-e15b0496bb37449fa91b82ed8f7a3f58 |
| Source note | uspto-grants-2002_09 |