HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663363Generated: October 25, 2026
5-Propylcyclohexane-1,3-dione → 4-[3-Bromo-4-(3-methoxy-benzyloxy)-5-nitro-phenyl]-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carbonitrile
https://huagongshe.com/reaction/1663363
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Propylcyclohexane-1,3-dione | HCID 2737224 | — |
| Reactant | 3-Aminocrotonitrile | HCID 5324720 | — |
| Reactant | 3-Bromo-4-(3-methoxy-benzyloxy)-5-nitro-benzaldehyde | HCID 86625158 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[3-Bromo-4-(3-methoxy-benzyloxy)-5-nitro-phenyl]-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carbonitrile | HCID 11949649 | — |
Reaction Steps
A mixture of 3-bromo-4-(3-methoxy-benzyloxy)-5-nitro-benzaldehyde (50 mg), 3-aminocrotonitrile (13 mg) and 5-propylcyclohexane-1,3-dione (25 mg) in 10 ml of ethanol was stirred at 80° C. for 17 h. The mixture was concentrated in vacuo. The residue was purified by chromatography on silicagel in heptane/ethyl acetate 8/2→1/1 (v/v) as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034945B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-9c6cb09aada94387b3abdea5423bd469 |
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| Source note | uspto-grants-2011_10 |
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