HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398019Generated: October 29, 2026
Hydrochloric Acid → HCID 23001738, compound
https://huagongshe.com/reaction/398019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 23001737 | HCID 23001737 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23001738 | HCID 23001738 | — |
Reaction Steps
7-Ethoxy-2′-methoxyflavone (7.4 g, 0.025 mol) was agitated in dichloromethane (100 ml). Boron tribromide (9.4 g, 3.6 ml, 0.0375 mol) in dichloromethane (100 ml) was added dropwise for an hour. The agitation was continued at room temperature for 24 hours. The reaction mixture was poured onto a mixture of crushed ice (100 g) and 36% hydrochloric acid (10 ml). After stirring the mixture for an hour, the precipitate was filtered off. 2.15 g (29%) of unreacted 7-ethoxy-2′-methoxyflavone was recovered. The filtrate was evaporated under reduced pressure to remove dichloromethane. From the aqueous residue, crude 7-ethoxy-2′-hydroxyflavone was obtained by filtration. The crude product was dried, thoroughly pulverized and treated with boiling chloroform for half an hour. The undissolved product was collected by filtration from the cooled mixture; and the crude 7-ethoxy-2′-hydroxyflavone was crystallized from dimethylformamide to give 3.10 g (43.9%) (m.p.: 295-297° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610738B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-a25eb729adc849ac9cc0488218527f37 |
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| Source note | uspto-grants-2003_08 |
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