HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(2,3,5-Trimethylphenoxy)butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(2,3,5-Trimethylphenoxy)butyrate | HCID 22000914 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2,3,5-Trimethylphenoxy)butanoic acid | HCID 14492659 | 53.8% |
Reaction Steps
A mixture of 4-(2,3,5-trimethylphenoxy)butyrate (9.09 g), 1N NaOH (58 ml), and EtOH (80 ml) was stirred at room temperature overnight. The reaction mixture was poured into a mixture of Et2O and water. The separated water phase was washed with Et2O, and was acidified by 6N HCl. After extraction by AcOEt, the AcOEt was washed with water and brine, and dried over MgSO4, and then evaporated. The resulting precipitate was collected by filtration, and dried to give 4-(2,3,5-trimethylphenoxy)butyric acid (4.91 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06225480B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-61632a7188a643998fb8733d69e7b5f9 |
| Source note | uspto-grants-2001_05 |