HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(p-Heptyloxybenzyloxy)-1-methoxy-2-indaneacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 5-(p-heptyloxybenzyloxy)-1-methoxy-2-indaneacetate | HCID 53634688 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(p-Heptyloxybenzyloxy)-1-methoxy-2-indaneacetic acid | HCID 19882677 | 72.7% |
Reaction Steps
In 1 ml of tetrahydrofuran and 8 ml of methanol were dissolved 220 mg of ethyl 5-(p-heptyloxybenzyloxy)-1-methoxy-2-indaneacetate obtained in Example 4. After 1 ml of a 5% aqueous sodium hydroxide solution was added to the solution, the mixture was stirred at room temperature for 8 hours. After diluting with water, the system was rendered acidic with hydrochloric acid followed by extraction with ethyl acetate. The ethyl acetate layer was washed with water, dried and concentrated. The obtained crystalline residue was recrystallized from ether-pentane to obtain 150 mg of 5-(p-heptyloxybenzyloxy)-1-methoxy-2-indaneacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994479 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-0df0b59809f54b6d9df1e610d2b9ad57 |
| Source note | uspto-grants-1991_02 |