HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 86605727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86605728 | HCID 86605728 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86605727 | HCID 86605727 | 94.4% |
Reaction Steps
To a solution of ethyl (3-{4-[(4-formyl-2-methoxyphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}phenyl)acetate (13.91 g) in tetrahydrofuran (200 mL)-ethanol (20 mL) was gradually added sodium borohydride (640 mg) at 0° C. After stirring at room temperature for 2 hrs, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated to give ethyl (3-{4-[(4-hydroxymethyl-2-methoxyphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}phenyl)acetate as colorless crystals (13.20 g, yield 94%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 96-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368578B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-d577a5548f5c44d0bd8ff0c70092cc14 |
| Source note | uspto-grants-2008_05 |