Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Reactant | HCID 53888831 | HCID 53888831 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11046131 | HCID 11046131 | 70% |
Reaction Steps
Sodium hydride (60% in oil, 0.32 g) was added, in small portions at 0° C., to a solution of diethyl cyanomethylphosphonate (1.3 g) in tetrahydrofuran (50 ml). The mixture was stirred for 15 minutes at the same temperature, to which was then added 4-(5-methyl-2-phenyl-4-oxazolylmethoxy)cinnamoaldehyde (2.0 g), followed by stirring for 30 minutes under ice-cooling. The reaction mixture was poured into water, which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), which was then concentrated to give (E,E)-5-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]-2,4-pentadienenitrile (1.5 g, 68%). Recrystallization of the product from ethyl acetate--hexane afforded colorless needles, m.p.120°-121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591862 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-1012e6975189454482bf819935c6a8de |
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| Source note | uspto-grants-1997_01 |
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