HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659315Generated: November 2, 2026
2'-Hydroxyacetophenone → HCID 20560229, compound
https://huagongshe.com/reaction/1659315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2'-Hydroxyacetophenone | HCID 8375 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-[benzyl(methyl)amino]acetate | HCID 11031023 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20560229 | HCID 20560229 | 74.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04303656 |
|---|
| Source dataset | uspto-grants-1981_12 |
|---|
| ORD ID | ord-4595d5e236714f0b847280a587a8d339 |
|---|
| Source note | uspto-grants-1981_12 |
|---|