Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193334Generated: October 31, 2026

Benzylamine → tert-Butyl 4-(2-(benzylamino)ethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1193334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl 4-(2-((methanesulfonyl)oxy)ethyl)piperidine-1-carboxylateHCID 15229596—
SolventTolueneHCID 1140—
Producttert-Butyl 4-(2-(benzylamino)ethyl)piperidine-1-carboxylateHCID 6679924943%

Reaction Steps

Benzylamine (345 μl, 3.22 mmol, 1.1 eq) was added to a solution of tert-butyl 4-(2-(methyl-sulfonyloxy)ethyl)piperidine-1-carboxylate (0.9 g, 2.93 mmol, 1 eq) and triethylamine (0.8 ml, 5.86 mmol, 2 eq) in toluene (50 ml), and refluxing was carried out for 48 h. After monitoring by thin-layer chromatography, the reaction solution was concentrated and the residue was taken up in ethyl acetate (100 ml), washed with water (30 ml) and sat. NaCl solution (40 ml), dried over sodium sulfate and concentrated under reduced pressure. After purification by column chromatography (silica gel, ethyl acetate), a yellow solid was obtained. Yield: 43% (400 mg, 1.25 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-7facf08e13494e999317230af450ba91
Source noteuspto-grants-2014_03