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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1719421Erstellt: 25. Oktober 2026

Bis(2-bromoethyl) ether → 4-[[8-Acetyl-7-[2-(2-bromoethoxy)ethoxy]-2-naphthalenyl]oxy]butanoic acid methyl ester

https://huagongshe.com/reaction/1719421

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis(2-bromoethyl) etherHCID 21521—
EduktSodium hydrideHCID 24758—
Edukt4-[(8-Acetyl-7-hydroxy-2-naphthalenyl)oxy]butanoic acid methyl esterHCID 54407199—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[[8-Acetyl-7-[2-(2-bromoethoxy)ethoxy]-2-naphthalenyl]oxy]butanoic acid methyl esterHCID 5366069154%

Reaktionsschritte

Under an argon atmosphere, 2 g (0.007 mol) of 4-[(8-acetyl-7-hydroxy-2-naphthalenyl)oxy]-butanoic acid methyl ester in 5 ml of anhydrous dimethylformamide was added to a suspension of 0.29 g of sodium hydride in 25 ml of anhydrous dimethylformamide. The mixture was stirred at room temperature for 20 minutes and then 7.7 g of bis-(2-bromoethyl)ether was added and the mixture was stirred at room temperature for 20 hours. The solvent was removed and residual oil was purified by high pressure liquid chromatography using 25% ethyl acetate-hexane to yield 1.6 g (54%) of 4-[[8-acetyl-7-[2-(2-bromoethoxy)ethoxy]-2-naphthalenyl]oxy]butanoic acid methyl ester as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04539419
Quelldatensatzuspto-grants-1985_09
ORD IDord-b5d7ee48ec8043edbc605fcd26c290b3
Quellennotizuspto-grants-1985_09