HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007926Generated: November 3, 2026
Sodium Hydroxide → 2-(2-(1-Benzothiophene-5-yl)ethoxy)acetic acid
https://huagongshe.com/reaction/1007926
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(2-Benzo[b]thiophen-5-ylethoxy)-1-piperidino-1-ethanone | HCID 22666374 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-(1-Benzothiophene-5-yl)ethoxy)acetic acid | HCID 21990058 | 74.6% |
Reaction Steps
In a mixture of 58 mL of ethanol and 6 mL of water is dissolved 6.40 g of 2-(2-benzo[b]thiophen-5-ylethoxy)-1-piperidino-1-ethanone, to which is added 1.27 g of sodium hydroxide. The mixture is heated under reflux for 4 hours. After cooling the mixture, the deposited matter is collected by filtration. The deposited matter is added to a mixture of ethyl acetate and water, pH is adjusted to 1.5 with 2 mol/L hydrochloric acid, 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, and the solvent is distilled off under reduced pressure to obtain 3.72 g of 2-(2-benzo[b]thiophen-5-ylethoxy)-acetic acid as a colorless crystalline 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-0b252585547a46fe8a2240492bf34990 |
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| Source note | uspto-grants-2004_09 |
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