Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377157Generated: October 26, 2026

Water → 1-(3-(2-(1-Benzothiophene-5-yl)ethoxy)propyl)-3-pyrrolidinol

https://huagongshe.com/reaction/2377157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-HydroxypyrrolidineHCID 98210—
Reactant5-[2-(3-Chloropropyloxy)ethyl]benzo[b]thiopheneHCID 21990069—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(3-(2-(1-Benzothiophene-5-yl)ethoxy)propyl)-3-pyrrolidinolHCID 2199003754.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

In 12 mL of N,N-dimethylformamide was dissolved 1.20 g of 5-[2-(3-chloropropoxy)ethyl]-1-benzothiophene, and 0.82 g of 3-pyrrolidinol and 1.30 g of potassium carbonate were added to the solution, after which the resulting mixture was stirred at 85° C. for 2.5 hours. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform : methanol 20:1 to 10:1) to obtain 0.78 g of 1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-pyrrolidinol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468443B2
Source datasetuspto-grants-2008_12
ORD IDord-00ab880a920c4cc98bafb2f73b92c8a6
Source noteuspto-grants-2008_12