HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 71903Erstellt: 24. Oktober 2026
Trifluoroacetic anhydride → 3,8-Dibromo-benzo[c]chromen-6-one
https://huagongshe.com/de/reaction/71903
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trifluoroacetic anhydride | HCID 9845 | — |
| Edukt | Carbamide Peroxide | HCID 31294 | — |
| Edukt | 2,7-Dibromo-9-fluorenone | HCID 259922 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3,8-Dibromo-benzo[c]chromen-6-one | HCID 59561042 | 134,5% |
Reaktionsschritte
A solution of TFAA (2.1 mL, 3.15 mmol) in dichloromethane (5 mL) was added dropwise to a suspension of 2,7-dibromo-fluoren-9-one (3.3 g, 10 mmol) and H2O2-urea (1.4 g, 15 mL) in dichloromethane (50 mL). The mixture was stirred at room temperature for 48 hours, a second portion of H2O2-urea was added, and stirring was continued at room temperature for a further 72 hours. The mixture was filtered, the organic phase was extracted with water (50 mL), and dried over Na2SO4. After removal of solvent, the residue was heated with 2N NaOH at 80° C. for 10 minutes, filtered, the cooled filtrate extracted with ether. The aqueous phase was acidified with 2N HCl and extracted with ethyl acetate (200 mL). HCl (2 mL 4M solution) was added to the ethyl acetate and heated for 2 hours. The solvent was removed under vacuum, the residue was recrystallized from ethyl acetate/ethanol to give the final product 3,8-Dibromo-benzo[c]chromen-6-one as a white solid (1.5 g, 40%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822430B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-d0fd6578ca784ef29ae53866540322c9 |
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| Quellennotiz | uspto-grants-2014_09 |
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