Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007899Generated: October 25, 2026

Hydrochloric Acid → N-[3-(2-benzo[b]thiophen-5-ylethoxy)propyl]-N,N-diethylamine

https://huagongshe.com/reaction/1007899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantDiethylamineHCID 8021—
Reactant5-[2-(3-Chloropropyloxy)ethyl]benzo[b]thiopheneHCID 21990069—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-[3-(2-benzo[b]thiophen-5-ylethoxy)propyl]-N,N-diethylamineHCID 22666289—

Reaction Conditions

Temperature100 °C

Reaction Steps

In 6 mL of N,N-dimethylformamide is dissolved 0.80 g of 5-[2-(3-chloropropyloxy)ethyl]benzo[b]-thiophene, to which is added 3.2 mL of diethylamine. The mixture is stirred in an ampoule at 100° C. for 10 hours. After cooling, the reaction mixture is introduced into a mixture of water and ethyl acetate, pH is adjusted to 1.0 with 6 mol/L hydrochloric acid, and the aqueous layer is separated. Ethyl acetate is added to the aqueous layer, pH is adjusted to 10.0 with 5 mol/L aqueous solution of sodium hydroxide, and the organic layer is separated. The organic layer is washed with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, the solvent is distilled off under reduced pressure, and the residue is purified by column chromatography (eluent: chloroform:methanol=10:1 to 4:1). Thus, 0.48 g of N-[3-(2-benzo[b]thiophen-5-ylethoxy)propyl]-N,N-diethylamine is obtained as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797726B1
Source datasetuspto-grants-2004_09
ORD IDord-4a8da577d4194a3789bebcea626b4cf3
Source noteuspto-grants-2004_09