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HRID 32199Erstellt: 23. Oktober 2026

Allyl bromide → 1-Allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine

https://huagongshe.com/de/reaction/32199

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl bromideHCID 7841—
EduktPotassium CarbonateHCID 11430—
EduktSodium BicarbonateHCID 516892—
Edukt1-[2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]piperazineHCID 11992284—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethane ethylacetateHCID 21226138—
Produkt1-Allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazineHCID 23141803—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 1-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine (30 mg, 0.1 mmol) produced in Example (8b), allyl bromide (14.8 mg, 0.12 mmol), potassium carbonate (20.8 mg, 0.15 mmol) and dimethylformamide (1 mL) was stirred for 4 hours and 20 minutes at an external temperature of 80° C. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with ethyl acetate-dichloromethane. The separated organic layer was washed with water, and then the solvent was distilled off by nitrogen stream. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 1-allyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425554B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-00d379097aaf48f39b85028bf376efd8
Quellennotizuspto-grants-2008_09