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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83826Generated: October 25, 2026

Dabco → 1-(2-(Tert-butoxycarbonylamino)ethyl)-4-aza-1-azonia-bicyclo[2.2.2]octane bromide

https://huagongshe.com/reaction/83826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDabcoHCID 9237—
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
SolventDiethyl EtherHCID 3283—
Product1-(2-(Tert-butoxycarbonylamino)ethyl)-4-aza-1-azonia-bicyclo[2.2.2]octane bromideHCID 6723530870%

Reaction Steps

To a solution of 1,4-diazabicyclo[2.2.2]octane (0.40 g, 3.57 mmol) in ether (5 mL) was added tert-butyl 2-bromoethylcarbamate (0.80 g, 3.57 mmol). The reaction was stirred overnight and the solvent was removed in vacuo. EtOAc (10 mL) was added and the reaction was stirred vigorously overnight. The precipitates were collected by filtration to give 1-(2-(tert-butoxycarbonylamino)ethyl)-4-aza-1-azonia-bicyclo[2.2.2]octane bromide (0.84 g) as a white solid. The solids were dissolved in MeOH (3 mL) and 4 M HCl in dioxane (3.5 mL, 14 mmol). The reaction was stirred at room temperature until it was determined to be complete by LCMS. The mixture was filtered to afford 1-(2-aminoethyl)-4-aza-1-azoniabicyclo[2.2.2]octane chloride hydrochloride (0.74 g) as a white solid. 1H-NMR (D2O, 400 MHz) δ 3.98-3.72 (m, 8H), 3.79-3.69 (m, 6H), 3.66-3.61 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846739B2
Source datasetuspto-grants-2014_09
ORD IDord-9e5f55bc6f7d4143ae246fbcfb38ecfb
Source noteuspto-grants-2014_09