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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256623Generated: October 26, 2026

Cycloheptylamine → N-Cycloheptyl-[(2-phenanthrenyl)methyl]amine

https://huagongshe.com/reaction/256623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCycloheptylamineHCID 2899—
ReactantPotassium CarbonateHCID 11430—
Reactant2-MethylphenanthreneHCID 17321—
ReactantN-bromobutanimideHCID 67184—
SolventDimethylformamideHCID 6228—
ProductN-Cycloheptyl-[(2-phenanthrenyl)methyl]amineHCID 1528429066.9%

Reaction Steps

2-Methylphenanthrene (2.00 g, 10.4 mmol) was brominated with N-bromosuccinimide (2.05 g, 11.5 mmol) and the product compound was added gradually to a suspension of cycloheptylamine (2.38 g, 21.0 mmol) and potassium carbonate (2.90 g, 21.0 mmol) in dimethylformamide (20 ml) with ice-cooling. The mixture was then stirred at room temperature for 16 hrs and, then, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 2.11 g of a viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258405
Source datasetuspto-grants-1993_11
ORD IDord-450d9398ff814e4c9fe9af5967e21e18
Source noteuspto-grants-1993_11