HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Methyl [4-(4-methoxybenzoyl)-2-methylphenoxy]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | HCID 13966818 | HCID 13966818 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl [4-(4-methoxybenzoyl)-2-methylphenoxy]acetate | HCID 13966816 | — |
Reaction Steps
50 g of 4-hydroxy-3-methyl-4'-methoxybenzophenone (R. Martin et al. Monatsh. Chemie 110, 1057-1066 (1979)) are dissolved in 200 ml of dry DMF and, under N2, 9 g of a 55% dispersion of sodium hydride in mineral oil are cautiously added. Then, while stirring, 19.5 ml of methyl bromoacetate are added dropwise, and the mixture is left to stand at room temperature overnight. The precipitated salt is filtered off with suction, and the filtrate is concentrated in vacuo. The residue is taken up in ethyl acetate, and the solution is washed with sodium bicarbonate solution and water. The organic phase is dried over magnesium sulfate, and the solvent is removed in vacuo. The residue is triturated with ether, filtered off with suction and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04922015 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-b62a71e5efb74246af51a330d376a20e |
| Source note | uspto-grants-1990_05 |