HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885722Generated: November 2, 2026
1,4-Naphthoquinone → HCID 15052363, compound
https://huagongshe.com/reaction/1885722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Naphthoquinone | HCID 8530 | — |
| Reactant | Levulinic Acid | HCID 11579 | — |
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15052363 | HCID 15052363 | — |
Reaction Steps
Naphthoquinone (3.12 g, 20 mmol), 4-oxopentanoic acid (13.9 g, 120 mmol) and silver nitrate (2.0 g, 11.8 mmole) are combined in 30% aqueous acetonitrile at 65° C. A solution of ammonium peroxydisulfate (12.0 g, 52.6 mmole) is added dropwise over 30 minutes while the stirred mixture is maintained at 65°-75° C. On cooling, the mixture is extracted with diethyl ether (300 ml). The extract is then washed with water (3×50 ml), 5% NaHCO3 (2×50 ml) and brine (50 ml) and dried over MgSO4. After filtration through active carbon, the ether solution is evaporated to give crude 2,3-bis(3-oxobutyl)-1,4-naphthoquinone which is recrystallized from aqueous ethanol to give 1.45 g product, mp 110°-112° C. This 2,3-bis(3-oxobutyl)-1,4-naphthoquinone (0.456 g, 1.53 mmole), aminoguanidine hydrochloride (0.46 g, 4.3 mmole) and a drop of concentrated HCl are combined in 5 ml of 90% ethanol and heated at reflux for 3 hours. On cooling, 2,3-bis(3-(2-amidinohydrazono)butyl)-1,4-naphthoquinone crystallizes from the reaction mixture, and recrystallization from ethanol gives 400 mg product, mp 181°-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05145975 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-7e926c329b9c42f18385f2f5e8200c30 |
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| Source note | uspto-grants-1992_09 |
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