HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1855958Erstellt: 26. Oktober 2026
Methyl Ethyl Ketone → 3-Ethoxy-4-(2-bromoethoxy)benzyl alcohol
https://huagongshe.com/reaction/1855958
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl Ethyl Ketone | HCID 6569 | — |
| Edukt | 1,2-Dibromoethane | HCID 7839 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Ethyl vanillyl alcohol | HCID 597767 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 3-Ethoxy-4-(2-bromoethoxy)benzyl alcohol | HCID 54373355 | 79,5% |
Reaktionsschritte
While stirring a mixture of 30 g of 3-ethoxy-4-hydroxybenzyl alcohol, 125 g of anhydrous potassium carbonate, and 600 ml of methyl ethyl ketone, 168 g of 1,2-dibromoethane was added to the mixture, and the resultant mixture was refluxed for 48 hours with stirring. After cooling, the reaction mixture was filtered under suction and the filtrate was distilled under reduced pressure to provide a pale-yellow oily matter. The product was dissolved in 300 ml of ether and the solution was washed twice each with 50 ml of an aqueous 5% sodium hydroxide solution and then with 50 ml of water, dried with anhydrous sodium sulfate, and distilled under reduced pressure to provide a yellow oily matter. To the product was added 100 ml of a mixture of ether and petroleum ether of 1:1 by volume ratio to form crystals, which were recovered by filtration under suction to provide 39 g of 3-ethoxy-4-(2-bromoethoxy)benzyl alcohol having a melting point of 51°-53° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04217305 |
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| Quelldatensatz | uspto-grants-1980_08 |
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| ORD ID | ord-1e0cf119f1a54d89993c78493263f005 |
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| Quellennotiz | uspto-grants-1980_08 |
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