HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-(2-(1-Benzothiophen-5-yl)ethoxy)propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 21990147 | HCID 21990147 | — |
| Product | 3-(2-(1-Benzothiophen-5-yl)ethoxy)propionic acid | HCID 21990080 | — |
Reaction Steps
In 0.6 mL of acetic acid was dissolved 200 mg of 3-[2-(1-benzothiophen-5-yl)ethoxy]propiononitrile, followed by adding thereto 0.4 mL of water and 0.184 mL of sulfuric acid, and the resulting mixture was stirred at 90 to 100° C. for 1 hour. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; toluene ethyl acetate=3:1) to obtain 140 mg of 3-[2-(1-benzothiophen-5-yl)ethoxy]propionic acid as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468443B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-2d56498e45774d70b2b53b0764181cbe |
| Source note | uspto-grants-2008_12 |