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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695561Generated: November 2, 2026

HCID 136404568, compound → HCID 68792857, compound

https://huagongshe.com/reaction/1695561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 136404568HCID 136404568—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68792857HCID 68792857—

Reaction Conditions

Temperature60 °C

Reaction Steps

In a 100 mL autoclave, dissolve 0.9 g of equimolecular mixture of the Z and E isomers of 4-(quinolin-2-yl)-fluoren-9-one oxime, obtained in Stage 3, in a mixture of 40 mL of ethanol and 40 mL of tetrahydrofuran, add a spatula tip of Raney nickel, then submit to an initial hydrogen pressure of 1 bar and heat the autoclave at 60° C. for 2 hours. After cooling, filter the catalyst on Celite and concentrate the filtrate at reduced pressure. After purification by flash chromatography on silica gel (20-40 μm), eluting with a mixture of dichloromethane and methanol (95-05 by volume), we obtain 0.72 g of 4-(quinolin-2-yl)-9H-fluoren-9-(R,S)-yl-amine in the form of a white meringue with the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163750B2
Source datasetuspto-grants-2012_04
ORD IDord-e9c4e775a6534c32b2706d452ce5c6b1
Source noteuspto-grants-2012_04