HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986481Generated: October 25, 2026
Piperidine → 2-(3,5-Dibromo-4-hydroxyphenyl)-6-hydroxy-3-methyl-4H-1-benzopyran-4-one
https://huagongshe.com/reaction/986481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3,5-Dibromo-4-Hydroxybenzaldehyde | HCID 18100 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2',5'-Dihydroxypropiophenone | HCID 70312 | — |
| Reactant | 3',5'-Dibromo-6,4'-dihydroxy-3-methylflavanone | HCID 13650818 | — |
| Reactant | 3,3',5'-Tribromo-6,4'-dihydroxy-3-methylflavanone | HCID 21283899 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(3,5-Dibromo-4-hydroxyphenyl)-6-hydroxy-3-methyl-4H-1-benzopyran-4-one | HCID 128600 | — |
Reaction Steps
1.6 g of bromine in 6 ml of chloroform are added dropwise to a solution of 4.12 g of 3',5'-dibromo-6,4'-dihydroxy-3-methylflavanone (m.p. 200°-202°; obtainable by reaction of 2,5-dihydroxypropiophenone with 3,5-dibromo-4-hydroxybenzaldehyde in boiling ethanol in the presence of piperidine) in 55 ml of dioxane while stirring and irradiating (500 watt Agaphot lamp). The mixture is stirred for a further 30 minutes while cooling and irradiating, the usual working-up is carried out, and the resulting crude 3,3',5'-tribromo-6,4'-dihydroxy-3-methylflavanone is dissolved in 100 ml of ethanol. 15 ml of 10% aqueous potassium hydroxide solution are added, and the mixture is boiled for 5 minutes, cooled, poured on to ice and the usual working-up is carried out. 3',5'-Dibrom-6,4'-dihydroxy-3-methylflavone ("D") is obtained, m.p. 264°-265°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04713465 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-d4c6203d4710429b8fc2774f31ac37aa |
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| Source note | uspto-grants-1987_12 |
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