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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410199Generated: October 31, 2026

Iodine → HCID 56653338, compound

https://huagongshe.com/reaction/2410199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactantp-METHYLACETOPHENONEHCID 8500—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 3513573HCID 3513573—
ProductHCID 56653338HCID 56653338—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815940B2
Source datasetuspto-grants-2014_08
ORD IDord-1b686f938069488c865174a4377a241e
Source noteuspto-grants-2014_08