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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890392Generated: November 1, 2026

tert-Butyl piperazine-1-carboxylate → HCID 86664147, compound

https://huagongshe.com/reaction/1890392

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
Reactant5-Bromo-2-(trifluoromethyl)pyridineHCID 2761197—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 86664147HCID 86664147—

Reaction Steps

5-Bromo-2-trifluoromethyl-pyridine (1.0 mmol), piperazine-1-carboxylic acid tert-butyl ester (1.2 mmol), sodium tert-butoxide (1.65 mmol), tris-(dibenzylideneacetone)-dipalladium (0.022 mmol) and 2-(dicyclohexylphosphino)-biphenyl (0.064 mmol) are dissolved in dry toluene (5 mL) and the resulting mixture is irradiated in a monomode microwave oven for 30 minutes at 100° C. The reaction is then cooled down to room temperature and ethyl acetate is added (15 mL). The precipitate formed is filtered and the filtrate is concentrated under reduced pressure. The crude product thus obtained is taken up in a minimum volume of dichloromethane (2 mL) and is purified by chromatography over a short silica gel pad (diethyl ether as eluent) to afford the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507474B2
Source datasetuspto-grants-2013_08
ORD IDord-2a691e4fa1d8421d8f0dd328ae77911c
Source noteuspto-grants-2013_08