HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395647Generated: October 26, 2026
Methyl 2-(2-methyl-1-imidazolyl)-4-(4-trifluoromethylphenyl)-5-oxazolepropionate → 2-(2-Methyl-1-imidazolyl)-4-(4-trifluoromethylphenyl)-5-oxazolepropanol
https://huagongshe.com/reaction/395647
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2-(2-methyl-1-imidazolyl)-4-(4-trifluoromethylphenyl)-5-oxazolepropionate | HCID 23431813 | — |
| Reactant | (+)-Sodium potassium tartrate sesquihydrate | HCID 131724023 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-Methyl-1-imidazolyl)-4-(4-trifluoromethylphenyl)-5-oxazolepropanol | HCID 23431807 | 81% |
Reaction Steps
Methyl 2-(2-methyl-1-imidazolyl)-4-(4-trifluoromethylphenyl)-5-oxazolepropionate (1.00 g) was dissolved in toluene (15 ml). To the obtained solution was added dropwise a mixture of a 70% toluene solution (1.20 g) of sodium dihydrobis(2-methoxyethoxy)aluminate, and toluene (5 ml) at 0° C., which was stirred at 0° C. for 30 minutes. To the reaction mixture was carefully added a 10% aqueous solution of (+)-sodium potassium tartrate sesquihydrate (50 ml), which was stirred at room temperature for 1 hour. The precipitated crystals were filtered, washed in sequence with a 10% aqueous solution of (+)-sodium potassium tartratesesquihydrate, pure water and isopropyl ether, and air-dried to give crystals of 2-(2-methyl-1-imidazolyl)-4-(4-trifluoromethylphenyl)-5-oxazolepropanol (0.75 g, 81%). Recrystallization from ethyl acetate-isopropyl ether gave pale yellow prisms. Melting point 127-129° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06605629B1 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-81db22682af64d388d0d2a192485d45e |
|---|
| Source note | uspto-grants-2003_08 |
|---|