HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-(1-Ethoxyethoxy)phenyl)ethyl butyrate → 1-(4-(1-Ethoxyethoxy)phenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-(1-Ethoxyethoxy)phenyl)ethyl butyrate | HCID 54484855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 1-(4-(1-Ethoxyethoxy)phenyl)ethanol | HCID 54418499 | 90% |
Reaction Steps
In 210 ml of 1N ethanol solution of potassium hydroxide was dissolved 28 g (0.1 mole) of the R-form of 1-(4-(1-ethoxyethoxy)phenyl)ethyl butyrate obtained in Example 2 (i), (ii) or (iii), the mixture was reacted at room temperature over night, and the reaction mixture was concentrated under reduced pressure To the residue was added 200 ml of ether, and it was washed with 2N aqueous solution of sodium hydroxide 2 times and then with water 3 times. The resulting ether layer was dried with anhydrous magnesium sulfate and ether was distilled under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane=1/4) to give 18.9 g of R-form of 1-(4-(1-ethoxyethyoxy)phenyl)ethanol (yield: 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05053507 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-025c720f50414656a12d46e08c818d85 |
| Source note | uspto-grants-1991_10 |