Sodium hydride → Methyl [4-(4-methoxybenzoyl)-2-methylphenoxy]acetate

HRID 1649956Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1649956
[OH:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[CH:10][CH:9]=2)=[O:7])=[CH:4][C:3]=1[CH3:18].[H-].[Na+].Br[CH2:22][C:23]([O:25][CH3:26])=[O:24]>CN(C=O)C>[CH3:15][O:14][C:11]1[CH:12]=[CH:13][C:8]([C:6]([C:5]2[CH:16]=[CH:17][C:2]([O:1][CH2:22][C:23]([O:25][CH3:26])=[O:24])=[C:3]([CH3:18])[CH:4]=2)=[O:7])=[CH:9][CH:10]=1

Komponenten

5

Versuchsvorschrift

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.

Aufarbeitung

  1. waitthe mixture is left
  2. filtrationThe precipitated salt is filtered off with suction
  3. concentrationthe filtrate is concentrated in vacuo
  4. washthe solution is washed with sodium bicarbonate solution and water
  5. dry with materialThe organic phase is dried over magnesium sulfate
  6. customthe solvent is removed in vacuo
  7. customThe residue is triturated with ether
  8. filtrationfiltered off with suction
  9. customdried

Quellen und Nachweise

ORD-Eintrag
ord-b62a71e5efb74246af51a330d376a20e
Quelldatensatz
uspto-grants-1990_05
Patentnummer
US04922015

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