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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659315Generated: November 2, 2026

2'-Hydroxyacetophenone → HCID 20560229, compound

https://huagongshe.com/reaction/1659315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-HydroxyacetophenoneHCID 8375—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-[benzyl(methyl)amino]acetateHCID 11031023—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20560229HCID 2056022974.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of sodium hydride (16.4 g) in absolute dioxane (700 ml) stirred at 80° C., was slowly added a mixture of o-hydroxyacetophenone (31.0 g) and N-benzyl-N-methylglycine ethyl ester (40 g) in dioxane (100 ml), and the resulting solution was boiled for 19 hours before being evaporated in vacuo. The residue was dissolved in ethanol and the mixture was saturated with dry HCl and stirred at room temperature for 18 hours. After evaporation the residue was taken up in chloroform and washed with water. Evaporation of the dried organic extracts yielded an oil (40 g) which was chromatographed on alumina eluting with chloroform to give the title chromone as a yellow oil (17.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04303656
Source datasetuspto-grants-1981_12
ORD IDord-4595d5e236714f0b847280a587a8d339
Source noteuspto-grants-1981_12