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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37644Generated: October 26, 2026

Ethanol → N-Cycloheptyl-1-(2-fluorenyl)ethylamine

https://huagongshe.com/reaction/37644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantCycloheptylamineHCID 2899—
Reactant2-AcetylfluoreneHCID 69908—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
ProductN-Cycloheptyl-1-(2-fluorenyl)ethylamineHCID 1993613525.9%

Reaction Steps

2-Acetylfluorene (4.17 g, 20 mmol) and cycloheptylamine (2.38 g, 21 mmol) were heated together at 130° C. for 14 hrs and, then, distilled under reduced pressure. To the residue were added ethanol (20 ml) and sodium borohydride (0.76 g, 20 mmol) and the mixture was stirred at room temperature overnight. The mixture was then diluted with water (100 ml) and extracted with chloroform (80 ml×2 times). The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was then purified by silica gel column chromatography to give 1.58 g of the amine compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420348
Source datasetuspto-grants-1995_05
ORD IDord-bcd683ca1d504603831d112f5f722637
Source noteuspto-grants-1995_05