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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770705Generated: November 2, 2026

3-(((Benzyloxy)carbonyl)amino)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N,3-trimethylbutan-1-aminium 4-methylbenzenesulfonate → 3-Amino-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N,3-trimethylbutan-1-aminium 4-methylbenzenesulfonate

https://huagongshe.com/reaction/1770705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(((Benzyloxy)carbonyl)amino)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N,3-trimethylbutan-1-aminium 4-methylbenzenesulfonateHCID 86665519—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-Amino-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N,3-trimethylbutan-1-aminium 4-methylbenzenesulfonateHCID 86665520113.6%

Reaction Steps

Under a nitrogen atmosphere, palladium on carbon (10%, 200 mg) was added to a solution of 3-(((benzyloxy)carbonyl)amino)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N,3-trimethylbutan-1-aminium 4-methylbenzenesulfonate (0.93 g, 2.2 mmol) in 15 mL of methanol. The flask was degassed and placed under a hydrogen atmosphere, stirring for 18 hours at room temperature. The suspension was filtered through a pad of Celite® washing with methanol, and the filtrate was concentrated under reduced pressure to give a clear oil (700 mg, 2.5 mmol). 1H NMR (D2O, 400 MHz) δ 1.08 (s, 6H), 1.79-1.83 (m, 2H), 2.29 (s, 3H), 3.04 (s, 6H), 3.27 (s, 3H), 3.36-3.41 (m, 2H), 3.45-3.51 (m, 4H), 3.56-3.60 (m, 6H), 3.84 (br m, 2H), 7.26-7.28 (d, J=8.0 Hz, 2H), 7.57-7.60 (d, J=8.0 Hz, 2H). LRMS (ESI/APCI) m/z 277 [M]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248117B2
Source datasetuspto-grants-2016_02
ORD IDord-9fa9c7344c1f4313ba3cdf2c8f2baac1
Source noteuspto-grants-2016_02