Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-[2-[3-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]phenyl]acetate | HCID 68884503 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68884245 | HCID 68884245 | 87% |
Reaction Steps
To a mixture of methyl 2-[2-[3-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]phenyl]acetate (0.50 g), tetrahydrofuran (2 mL) and methanol (2 mL) was added a 1N aqueous sodium hydroxide solution (2.0 mL) and the mixture was stirred at 50° C. for 1 hr. 1N Hydrochloric acid (2 mL) and water were added to acidify the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated: to give crystals (0.41 g, 87%) of 2-[2-[3-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]phenyl]acetic acid. Recrystallization from methyl acetate-hexane gave colorless prism crystals. melting point: 117-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07238716B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-5568d42759864c38af5b14bf4ec51f4d |
|---|
| Source note | uspto-grants-2007_07 |
|---|