HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857525Generated: October 25, 2026
Sodium hydride → (Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxane
https://huagongshe.com/reaction/1857525
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide | HCID 2724168 | — |
| Reactant | 4-[2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy]benzaldehyde | HCID 10757106 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxane | HCID 11811571 | 77.3% |
Reaction Steps
Sodium hydride (60% in oil, 0.78 g) was added in limited amounts, at room temperature, to a solution of [2-(1,3-dioxan-2-yl)ethyl]triphenylphosphonium bromide (8.9 g) in N,N-dimethylformamide (100 ml). The mixture was stirred for 30 minutes at the same temperature range, to which was added 4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzaldehyde (5.0 g). The mixture was stirred for 15 minutes at room temperature, then for 5 hours at 70° C. The reaction mixture was poured into ice-water, which was acidified with 2N HC1,, followed by extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4). The residue was purified by means of a silica gel column chromatography. From the fractions eluted with hexane - ethyl acetate (3:1), (Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxane (5.1 g, 77%) was obtained as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06147099 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-c7225a0946fc4b59a7074d2030a8d595 |
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| Source note | uspto-grants-2000_11 |
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