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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856083Generated: October 30, 2026

tert-Butyl 4-(2-chloroethyl)piperazinecarboxylate → tert-Butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/856083

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(2-chloroethyl)piperazinecarboxylateHCID 22106269—
ReactantMonomethylamine methanolHCID 57454252—
SolventMethanolHCID 887—
Producttert-Butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylateHCID 2308139198%

Reaction Steps

Tert-butyl 4-(2-chloroethyl)piperazine-1-carboxylate (3.13 g, 12.58 mmol) was dissolved in methanol (20 ml), to which 40% methylamine methanol solution (30 ml) was added, and the mixture was heated under reflux for 5 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in methylene chloride. The mixture was washed with saturated sodium hydrogencarbonate aqueous solution. The organic layer was dried over magnesium sulfate, and then filtered, and the filtrate was concentrated under reduced pressure to afford tert-butyl 4-(2-methylaminoethyl)piperazine-1-carboxylate (3.0 g, yield 98%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-706d8394160b4315bd33841d9aca6d42
Source noteuspto-grants-2007_08