HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(2-Indenyl)-3-methylbutanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | m-Phenoxylbenzyl 2-(2-indenyl)-3-methylbutanoate | HCID 13146349 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Indenyl)-3-methylbutanoic acid | HCID 23347091 | — |
Reaction Steps
A mixture of m-phenoxybenzyl 2-(2-indenyl)-3-methylbutanoate (8 mmol), potassium hydroxide (24 mmol), ethanol (25 ml) and water (4 ml) is heated to reflux for about 3 hours. After cooling, the reaction is acidified with dilute hydrochloric acid. The mixture is extracted with ether, and the ether phase is washed to neutrality with saturated NaCl solution. Removal of solvent by evaporation yields 2-(2-indenyl)-3-methylbutanoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04217302 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-609db78ab8d241ce8b49aba049ae0309 |
| Source note | uspto-grants-1980_08 |