HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 6-{[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]methyl}-1-benzothiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 6-{[5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]methyl}-benzothiophene-2-carboxylate | HCID 59424234 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-{[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]methyl}-1-benzothiophene-2-carboxylic acid | HCID 57624565 | — |
Reaction Steps
A solution of ethyl 6-{[5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]methyl}-1-benzothiophene-2-carboxylate (70 mg, 0.18 mmol) in THF (2.5 mL) was treated with 1M KOH solution (0.89 mL, 0.89 mmol) and stirred at ambient temperature for 12 hours. The reaction was partitioned between 1M HCl and ethyl acetate. The organics were dried over sodium sulfate, filtered and evaporated to give the title compound as a white solid. LC/MS (EI): cal'd 367.0 (MH+), exp 367.0 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07834034B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-74f3594aad754130b3ee096d48674936 |
| Source note | uspto-grants-2010_11 |