HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Carboxy-7-(2,3-epoxypropoxy)benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 7-(2,3-Epoxypropoxy)-2-ethoxycarbonylbenzofuran | HCID 20211996 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Carboxy-7-(2,3-epoxypropoxy)benzofuran | HCID 13729412 | — |
Reaction Steps
There was dissolved 2.6 g (0.01 mole) of 7-(2,3-epoxypropoxy)-2-ethoxycarbonylbenzofuran obtained in Reference Example 9 in 10 ml of ethanol, and thereto 0.9 g (0.012 mole) of potassium hydroxide in 5 ml of ethanol solution was added dropwise with stirred under cooling with ice. After stirring the mixture for 3 hours the reaction was completed to neutralize the reaction mixture by 2N hydrochloric acid. Thereafter, the solvent was distilled away from the reaction mixture under reduced pressure, the resultant residue was extracted from 30 ml of chloroform. After washing the chloroform layer with water the layer was dried with magnesium sulfate, and then chloroform was distilled away under reduced pressure to give the resultant residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04652566 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-3bae652913854429b6fd373248e5a650 |
| Source note | uspto-grants-1987_03 |