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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7462Generated: October 25, 2026

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

https://huagongshe.com/reaction/7462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant3-[2-(1-Benzothiophen-5-yl)ethoxy]-1-propanolHCID 21990066—
SolventDichloromethaneHCID 6344—
Product5-[2-(3-Bromopropoxy)ethyl]-1-benzothiopheneHCID 2199007676.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087594B2
Source datasetuspto-grants-2006_08
ORD IDord-955645a8fc6a4fd1b0144ff9ec621f18
Source noteuspto-grants-2006_08