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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl Ethyl KetoneHCID 6569—
Edukt1,2-DibromoethaneHCID 7839—
EduktPotassium CarbonateHCID 11430—
EduktEthyl vanillyl alcoholHCID 597767—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-Ethoxy-4-(2-bromoethoxy)benzyl alcoholHCID 5437335579,5%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04217305
Quelldatensatzuspto-grants-1980_08
ORD IDord-1e0cf119f1a54d89993c78493263f005
Quellennotizuspto-grants-1980_08