Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | p-METHYLACETOPHENONE | HCID 8500 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 3513573 | HCID 3513573 | — |
| Product | HCID 56653338 | HCID 56653338 | — |
Reaction Steps
A solution of 5-tert-butyl-4-hydroxyisophthalaldehyde of formula I (0.50 g, 3.05 mmol) and p-methyl acetophenone (0.41 g, 3.05 mmol) in dioxane (25 mL) was treated with iodine (0.78 g, 0.31 mmol). The solution was heated at 90° C. for 5.0 h. Most of the excess reagent was evaporated under reduced pressure, and the residue was treated with aq. Na2S2O3 solution (5%, 40 mL) and the product was extracted 3-fold with CHCl3 (50 mL). The combined organic layers were dried on Na2SO4, filtered, and concentrated to dryness under reduced pressure. The residue was chromatographed over silica gel (SiO2, 230-400 flash), eluting with a gradient of 4% ethyl acetate in hexane, which upon concentration provides (E)-3-tort-butyl-2-hydroxy-5-(3-oxo-3-p-tolylprop-1-enyl)benzaldehyde (General Formula III).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815940B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-1b686f938069488c865174a4377a241e |
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| Source note | uspto-grants-2014_08 |
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