HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132990Erstellt: 25. Oktober 2026
Potassium Iodide → (4-Iodo-5-oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-1-yl)methyl acetate
https://huagongshe.com/reaction/132990
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Thallium(1+);2,2,2-trifluoroacetate | HCID 21902506 | — |
| Edukt | (5-Oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-1-yl)methyl acetate | HCID 58646841 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Trifluoroacetic acid | HCID 6422 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | (4-Iodo-5-oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-1-yl)methyl acetate | HCID 12150904 | — |
Reaktionsschritte
4.4 g of (5-oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-1-yl)methyl acetate prepared in Example 1-f was dissolved in 30 ml of trifluoroacetic acid, and 5.0 g of thallium trifluoroacetate was added at room temperature in an atmosphere of nitrogen gas. The mixture was stirred at room temperature for 4 hours, followed by stirring at 50° C. for 2 hours. After the starting material disappeared, 3 ml of an aqueous solution of 1.5 g of potassium iodide was added to the reaction mixture and the mixture was stirred at room temperature for 0.5 hour. To the reaction mixture were added ethyl acetate and water, and the mixture was neutralized with sodium hydrogencarbonate and filtered through Celite. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified and separated by silica gel column chromatography (ethyl acetate:hexane=1:20), to give 4.1 g of a 3:1 mixture of the title compounds as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07390797B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-beb1bafe3a1c4769af44e738bbebdf18 |
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| Quellennotiz | uspto-grants-2008_06 |
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