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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022913Generated: October 29, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 71146962, compound

https://huagongshe.com/reaction/1022913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Boc-4-methylpiperazineHCID 11401394—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71146962HCID 7114696246.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of tert-butyl 4-methylpiperazine-1-carboxylate (24.2 g), N,N,N′,N′-tetramethylethane-1,2-diamine (21 g) and tetrahydrofuran (500 mL) was cooled to −78° C. under a nitrogen atmosphere, and sec-butyllithium (184 mL, 1.3M cyclohexane solution) was added dropwise over 1.5 hr while stirring. Furthermore, the mixture was stirred at the same temperature for 2 hr, the reaction system was heated to 30° C., and the mixture was stirred for 1.5 hr. Thereafter, the reaction system was cooled again to −78° C., and a solution of 1-benzylpiperidin-4-one (28.3 g) in tetrahydrofuran (50 mL) was added dropwise over 1 hr. The reaction system was stirred at room temperature overnight, and the mixture was cooled to 0° C. Saturated aqueous ammonium chloride solution (100 mL) was added, and the mixture was stirred at room temperature for 30 min. The mixture was extracted with ethyl acetate (300 mL), and the extract was washed with water (300 mL) and dried over anhydrous sodium sulfate. Insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (17.6 g) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722660B2
Source datasetuspto-grants-2014_05
ORD IDord-b517c84136e144d5a06215ab8c92ac64
Source noteuspto-grants-2014_05