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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7462Erstellt: 23. Oktober 2026

Water → 5-[2-(3-Bromopropoxy)ethyl]-1-benzothiophene

https://huagongshe.com/de/reaction/7462

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktCarbon tetrabromideHCID 11205—
EduktTriphenylphosphineHCID 11776—
Edukt3-[2-(1-Benzothiophen-5-yl)ethoxy]-1-propanolHCID 21990066—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-[2-(3-Bromopropoxy)ethyl]-1-benzothiopheneHCID 2199007676,2%

Reaktionsschritte

In 40 mL of methylene chloride was dissolved 2.00 g of 3-[2-(1-benzothiophen-5-yl)ethoxy]-1-propanol, and 5.55 g of triphenylphosphine was added to the solution, after which a solution of 8.42 g of carbon tetrabromide in 10 mL of methylene chloride was added dropwise thereto under ice-cooling and the resulting mixture was stirred at room temperature for 20 minutes. To the reaction mixture was added 20 mL of water, and the organic layer was separated. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. Diethyl ether was added to the residue and the insoluble materials were filtered off, after which the solvent was distilled off under reduced pressure. The residue was purified by a column chromatography (eluent; hexane:ethyl acetate=20:1 to 10:1) to obtain 1.93 g of 5-[2-(3-bromopropoxy)ethyl]-1-benzothiophene as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087594B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-955645a8fc6a4fd1b0144ff9ec621f18
Quellennotizuspto-grants-2006_08