Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 21840259 | HCID 21840259 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21840248 | HCID 21840248 | 71.2% |
Reaction Steps
(5-Methyl-2-phenyl-4-oxazolylmethyl)triphenyl-phosphonium chloride (25.4 g) was added to a solution of sodium ethoxide in ethanol [prepared from sodium (1.4 g) and ethanol (300 ml)] under cooling. The mixture was stirred at room temperature for 5 minutes, and then 4-bromobenzaldehyde (10.0 g) was added. After stirring at room temperature for 2 hours, the reaction mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel. The fractions eluted with ether-hexane (1:20, v/v) gave (E)-4-[2-(4-bromophenyl)vinyl]-5-methyl-2-phenyloxazole (13.1 g, 71%). This product was recrystallized from ethyl acetate-hexane. Colorless prisms, mp: 138-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05965589 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-5a2997ba5c8347609618bd24edfb5461 |
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| Source note | uspto-grants-1999_10 |
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