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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280571Generated: October 25, 2026

tert-Butyl 1-(2,2,2-trifluoroethyl)piperidin-4-ylcarbamate → 1-(2,2,2-Trifluoroethyl)piperidin-4-amine

https://huagongshe.com/reaction/1280571

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 1-(2,2,2-trifluoroethyl)piperidin-4-ylcarbamateHCID 22562166—
Solvent1,4-DioxaneHCID 31275—
Product1-(2,2,2-Trifluoroethyl)piperidin-4-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451804B1
Source datasetuspto-grants-2002_09
ORD IDord-e15b0496bb37449fa91b82ed8f7a3f58
Source noteuspto-grants-2002_09