Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 22666344 | HCID 22666344 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 68796619 | HCID 68796619 | — |
Reaction Steps
In 8 mL of methylene chloride is dissolved 0.80 g of 2-[2-(6-methoxybenzo[b]thiophen-5-yl)ethoxy]-acetic acid, to which are added 1.38 mL of triethylamine and 0.22 g of imidazole. The mixture is cooled to 5° C., to which is dropwise added a mixture of 0.24 mL of thionyl chloride and 8 mL of methylene chloride. The resulting mixture is stirred at the same temperature as above for one hour. The reaction mixture is cooled to −60° C., 0.47 mL of triethylamine and 0.31 mL of 2-(methylamino)-ethanol are added thereto, and the resulting mixture is stirred at the same temperature as above for one hour and the at ambient temperature for 1.5 hours. Water is added to the reaction mixture, pH is adjusted to 1.0 with 6 mol/L hydrochloric acid, and the organic layer is separated. The organic layer is washed with saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. Thus, 0.93 g of N1-(2-hydroxyethyl)-N1-methyl-2-[2-(6-methoxybenzo[b]thiophen-5-yl)ethoxy]-acetamide 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-c6b5f2a8c602417ea1905772ffda67a6 |
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| Source note | uspto-grants-2004_09 |
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