HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462523Generated: November 1, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 6-(4-Chloro-1-butenyl)carbostyril
https://huagongshe.com/reaction/1462523
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | 6-(4-Chloro-1-butenyl)-3,4-dihydrocarbostyril | HCID 54437579 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-(4-Chloro-1-butenyl)carbostyril | HCID 54172106 | — |
Reaction Steps
2.5 Grams of 6-(4-chloro-1-butenyl)-3,4-dihydrocarbostyril and 2.3 g of DDQ (2,3-dichloro-5,6-dicyanobenzoquinone) were mixed in 160 ml of dioxane and the mixture was refluxed by heating for 6 hours. Further, 1.1 of DDQ was added to the reaction mixture and the mixture was refluxed by heating for 3 hours. The reaction mixture was cooled and the precipitates thus formed were removed by filtration and the motor liquor was concentrated under a reduced pressure to obtain a residue. The residue was dissolved in a mixture of 100 ml of chloroform with 5 ml of methanol and the solution was padded through a silica gel column for removing the unreacted DDQ. The residue was recrystallized from methanol to obtain 1.6 g of 6-(4-chloro-1-butenyl)carbostyril in yellow needle-like crystals. Melting point: 215°-218° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04460593 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-b2b5b75acb134d27b42654905337ef2b |
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| Source note | uspto-grants-1984_07 |
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