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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364735Generated: October 27, 2026

Triethylamine → Tert-butyl 4-(cyclopropylmethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2364735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromomethylcyclopropaneHCID 81503—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(cyclopropylmethyl)piperazine-1-carboxylateHCID 4674308262.5%

Reaction Steps

Tert-butyl piperazine-1-carboxylate 7a (6.14 g, 33 mmol), bromomethyl-cyclopropane (4.05 g, 30 mmol) and triethylamine (6.06 g, 60 mmol) were dissolved in 70 mL of dichloromethane. The reaction solution was stirred for 12 hours. The resulting solution was added with 50 mL of aqeuous saturated sodium bicarbonate solution and extracted with dichloromethane (50 mL×3). The combined organic phase was washed with saturated sodium chloride solution (50 mL), dried over anhydrous magnesium sulfate. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound tert-butyl 4-(cyclopropylmethyl)piperazine-1-carboxylate 31a (4.50 g, yield: 62.5%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-a4e7fcf06ce94149969077785e235f67
Source noteuspto-grants-2014_04