HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-Bromo-5-phenylthiophene-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Bromo-5-phenyl-thiophene-3-carboxylic acid ethyl ester | HCID 58110272 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-5-phenylthiophene-3-carboxylic acid | HCID 58110310 | 87% |
Reaction Steps
Potassium hydroxide (0.65 g, 11.6 mmol) in water (2 mL) was added to a solution of 2-bromo-5-phenyl-thiophene-3-carboxylic acid ethyl ester (3.9 mmol) in IMS (6 mL). The reaction was stirred for 1 hour and then partitioned between diethyl ether and water. The aqueous layer was acidified to pH 7 with 1 N hydrochloric acid and further extracted with diethyl ether. The organic solution was dried over magnesium sulfate, filtered and the solvent evaporated to give the title compound (0.96 g, 87%). LCMS m/z 281.97 [M−H]− R.T.=3.64 min. (Analytical Method 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08614209B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-c662300dae1e4066917c421fb4d88319 |
| Source note | uspto-grants-2013_12 |