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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007933Generated: October 30, 2026

Water → N-[2-(2-benzo[b]thiophen-5-ylethoxy)ethyl]-N-(2-propynyl)amine

https://huagongshe.com/reaction/1007933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPropargylamineHCID 239041—
Reactant2-(2-Benzo[b]thiophen-5-ylethoxy)ethyl methanesulfonateHCID 21990050—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-[2-(2-benzo[b]thiophen-5-ylethoxy)ethyl]-N-(2-propynyl)amineHCID 22666513—

Reaction Conditions

Temperature80 °C

Reaction Steps

In 15 mL of N,N-dimethylformamide is dissolved 3.00 g of 2-(2-benzo[b]thiophen-5-ylethoxy)-ethyl methanesulfonate, to which are added 1.40 mL of propargylamine and 2.76 g of potassium carbonate. The mixture is heated at 80° C. for 3 hours. The reaction mixture is introduced into a mixture of water and ethyl acetate, and the organic layer is separated. The organic layer is washed with water and saturated aqueous solution of sodium chloride successively 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=30:1 to 20:1) to obtain 1.63 g of N-[2-(2-benzo[b]thiophen-5-ylethoxy)ethyl]-N-(2-propynyl)amine as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797726B1
Source datasetuspto-grants-2004_09
ORD IDord-b4c0ac5b5c144bd4afa623bb7a232fb6
Source noteuspto-grants-2004_09