HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-[4-(4-Carboxy-1-oxabutyl)phenyl]-4,5,6,7-tetramethoxy-2-indancarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-[4-(4-ethoxycarbonyl-1-oxabutyl)phenyl]-4,5,6,7-tetramethoxy-2-indancarboxylate | HCID 18348634 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[4-(4-Carboxy-1-oxabutyl)phenyl]-4,5,6,7-tetramethoxy-2-indancarboxylic acid | HCID 18348531 | 98.4% |
Reaction Steps
An aqueous sodium hydroxide solution (3 N, 0.440 ml, 1.32 mmols) was added to an ethanol (4 ml) solution of ethyl 2-[4-(4-ethoxycarbonyl-1-oxabutyl)phenyl]-4,5,6,7-tetramethoxy-2-indancarboxylate (342 mg, 0.662 mmols), and heated under reflux for 6 hours. The reaction mixture was concentrated in vacuo, diluted with water, made acidic by adding 10% hydrochloric acid, and then extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, and then dried. The solvent was evaporated out, and the resulting crude product was purified by recrystallization (from hexane-ethyl acetate) to obtain the entitled compound (300 mg) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06326369B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-5dc831d02d724274a8b5f004692b15dc |
| Source note | uspto-grants-2001_12 |