HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1161491Erstellt: 24. Oktober 2026
Bromochloromethane → 2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene
https://huagongshe.com/de/reaction/1161491
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromochloromethane | HCID 6333 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Edukt | 4-Bromo-2-(2-hydroxyethyl)-6-methoxyphenol | HCID 67097474 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene | HCID 59517213 | 44,6% |
Reaktionsschritte
To a solution of 898 mg of 4-bromo-2-(2-hydroxyethyl)-6-methoxyphenol in 10 ml of DMF there was added 1 g of sodium bistrimethylsilylamide while cooling on ice, and the mixture was stirred at room temperature for 30 minutes. After adding 1 ml of bromochloromethane to the reaction mixture, it was stirred at 80° C. for 20 hours under a nitrogen atmosphere. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (420 mg) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07816522B2 |
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| Quelldatensatz | uspto-grants-2010_10 |
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| ORD ID | ord-9fcb4ee3f48e46589890d7e06171e541 |
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| Quellennotiz | uspto-grants-2010_10 |
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