HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007893Generated: October 31, 2026
Water → N-[2-(2-benzo[b]thiophen-5-ylethoxy)ethyl]-N,N-dipropylamine
https://huagongshe.com/reaction/1007893
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dipropylamine | HCID 8902 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2-Benzo[b]thiophen-5-ylethoxy)ethyl methanesulfonate | HCID 21990050 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[2-(2-benzo[b]thiophen-5-ylethoxy)ethyl]-N,N-dipropylamine | HCID 22666418 | — |
Reaction Steps
In 8 mL of N,N-dimethylformamide is dissolved 0.80 g of 2-(2-benzo[b]thiophen-5-ylethoxy)ethyl methanesulfonate, to which are added 0.73 mL of dipropylamine and 0.74 g of potassium carbonate. The resulting mixture is stirred 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 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). Thus, 0.60 of N-[2-(2-benzo[b]thiophen-5-ylethoxy)ethyl]-N,N-dipropylamine is obtained as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06797726B1 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-57cac10567b94557a233ed95646d8627 |
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| Source note | uspto-grants-2004_09 |
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