HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Acenaphtheneacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl2-(1,2-dihydro-1-acenaphthylenyl)acetate | HCID 13715672 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Acenaphtheneacetic acid | HCID 344519 | — |
Reaction Steps
The ester obtained in Step C (1.9 g, 7.91.10−3 mol) is heated at reflux in the presence of potassium hydroxide (2.34 g, 4.17.10−2 mol, 5.3 eq.), water (16 ml) and methanol (16 ml) for one night. After evaporating off the solvent, the residue is taken up in water and extracted twice with ether. The basic aqueous phase is acidified using concentrated HCl in the cold state. The acid is extracted with ethyl acetate and dried over MgSO4. After evaporating off the solvent under reduced pressure, the title compound is obtained in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06423870B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-05a60df93b1e44c8a9252e7aa4a4a5a4 |
| Source note | uspto-grants-2002_07 |