HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695561Generated: November 2, 2026
HCID 136404568, compound → HCID 68792857, compound
https://huagongshe.com/reaction/1695561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 136404568 | HCID 136404568 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68792857 | HCID 68792857 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163750B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-e9c4e775a6534c32b2706d452ce5c6b1 |
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| Source note | uspto-grants-2012_04 |
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