HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 22930722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86591674 | HCID 86591674 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22930722 | HCID 22930722 | 91% |
Reaction Steps
A mixture of methyl [1-methyl-3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzyloxy]-1H-pyrazol-4-ylacetate (379 mg), 1N aqueous sodium hydroxide solution (2 ml), tetrahydrofuran (4 ml) and ethanol (4 ml) was stirred at room temperature for 2 hrs. 1N Hydrochloric acid (2 ml) was added to the reaction mixture and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained colorless crystals were collected by filtration to give [1-methyl-3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzyloxy]-1H-pyrazol-4-yl]acetic acid (333 mg, yield 91%), which was then recrystallized from ethanol-hexane. melting point: 148–149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241785B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-0268fcdecd75434b8e389e093e4278df |
| Source note | uspto-grants-2007_07 |