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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098344Generated: November 2, 2026

Trifluoroacetic acid → 4-(4-Aminomethylpiperidin-1-ylmethyl)-piperidine-1-carboxylic acid methyl ester

https://huagongshe.com/reaction/1098344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-[4-(Tert-butoxycarbonylamino-methyl)piperidin-1-ylmethyl]-piperidine-1-carboxylic acid methyl esterHCID 66810903—
SolventDichloromethaneHCID 6344—
Product4-(4-Aminomethylpiperidin-1-ylmethyl)-piperidine-1-carboxylic acid methyl esterHCID 66810785—

Reaction Steps

To a solution of 4-[4-(tert-butoxycarbonylamino-methyl)piperidin-1-ylmethyl]-piperidine-1-carboxylic acid methyl ester (4.4 g, 10.8 mmol) in dichloromethane (20 mL) was added trifluoroacetic acid (20 mL). After stirring for 20 min at room temperature, the solution was evaporated in vacuo, yielding the bis-trifluoroacetate salt of the title compound as a pale yellow oil, which was used without further treatment. (m/z): [M+H]+ calcd for C14H27N3O2 270.22; found 270.5. 1H-NMR (CD3OD) δ (ppm) 4.0 (br d, 2H), 3.6 (m, 5H), 2.9-2.7 (m, 6H), 2.1-1.9 (m, 2H), 1.7-1.5 (m, 6H), 1.2-1.0 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143279B2
Source datasetuspto-grants-2012_03
ORD IDord-b8977ab313a04162b3a7eae26b1e7093
Source noteuspto-grants-2012_03