HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-(2-(1-Benzothiophen-5-yl)ethoxy)propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Propyl 3-(2-(1-benzothiophen-5-yl)ethoxy)propionate | HCID 57615042 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-(1-Benzothiophen-5-yl)ethoxy)propionic acid | HCID 21990080 | 86.7% |
Reaction Steps
To methanol (12 mL) solution of 12.0 g of propyl 3-(2-(1-benzothiophen-5-yl)ethoxy)propionate was added water (12 mL) solution of 2.76 g of potassium hydroxide, which was then stirred at room temperature for 1.5 hours. This reaction mixture was distilled off under reduced pressure, to which were added 36 mL of toluene and 36 mL of water. The pH was adjusted to 1.9 with 8 mL of 6 mol/L hydrochloric acid. The organic layer was separated, followed by distilling off the solvent under reduced pressure. Thereto were added 12 mL of toluene and 24 mL of cyclohexane. The precipitate was collected by filtration to provide 8.91 g of 3-(2-(1-benzothiophen-5-yl)ethoxy)propionic acid as white solid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273902B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-c934b61e15eb4e9caeb31e0c2185daa8 |
| Source note | uspto-grants-2012_09 |