Methylparaben → Methyl 4-{[2-(dimethylamino)-2-oxoethyl]oxy}benzoate

HRID 1874666Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1874666
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Cl[CH2:19][C:20]([N:22]([CH3:24])[CH3:23])=[O:21]>CN(C=O)C>[CH3:23][N:22]([CH3:24])[C:20](=[O:21])[CH2:19][O:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:10][CH:11]=1

Komponenten

5

Versuchsvorschrift

Methyl 4-hydroxybenzoate (Fluka) (1.52 g, 10 mmol) and potassium carbonate (1.38 g, 10 mmol) in DMF (10 mL) was treated with 2-chloro-N,N-dimethylacetamide (Merck) (1.03 ml, 10 mmol) and the mixture was stirred at RT overnight. The reaction mixture was worked up by partitioning between ethyl acetate and 2M hydrochloric acid, washing with HCl, brine, dried (MgSO4) and evaporating to dryness. The residue was dissolved in DMF (5 mL) and treated with potassium carbonate (1.38 g, 10 mmol) and 2-chloro-N,N-dimethylacetamide (Merck) (1.03 ml, 10 mmol). The mixture was stirred at RT over the weekend, and then worked up. Partitioned between ethyl acetate and 2M HCl and the organic solution was washed with HCl (X2), brine (X3), dried (MgSO4), and evaporated to give the title compound (1.62 g, 68%) as a white solid. LCMS (System A) RT=0.73 min, ES+ve m/z 238 (M+H)+.

Aufarbeitung

  1. customby partitioning between ethyl acetate and 2M hydrochloric acid
  2. washwashing with HCl, brine
  3. dry with materialdried (MgSO4)
  4. customevaporating to dryness
  5. dissolutionThe residue was dissolved in DMF (5 mL)
  6. stirringThe mixture was stirred at RT over the weekend
  7. customPartitioned between ethyl acetate and 2M HCl
  8. washthe organic solution was washed with HCl (X2), brine (X3)
  9. dry with materialdried (MgSO4)
  10. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-b04181af892b4480bb12886a6abc2173
Quelldatensatz
uspto-grants-2012_11
Patentnummer
US08304446B2

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