Water → [(2,4-Difluoro-phenyl)-methyl-amino]-acetic acid methyl ester

HRID 2122086Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2122086
[F:1][C:2]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:3]=1[NH:4][CH3:5].C([O-])([O-])=O.[K+].[K+].Br[CH2:18][C:19]([O:21][CH3:22])=[O:20].O>CN1C(=O)CCC1>[CH3:22][O:21][C:19](=[O:20])[CH2:18][N:4]([C:3]1[CH:6]=[CH:7][C:8]([F:10])=[CH:9][C:2]=1[F:1])[CH3:5]

Komponenten

6

Edukt 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 60984Methyl bromoacetateHCID 27370232,4-difluoro-N-methylaniline

Produkt 1

HCID 20627003[(2,4-Difluoro-phenyl)-methyl-amino]-acetic acid methyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 13387N-methyl-2-pyrrolidoneLösungsmittel

Versuchsvorschrift

To a mixture of the 2,4-Difluoro-N-methylaniline (Avacado Research Chemical, Heysham UK) (1.43 g, 10 mmole) in NMP, and K2CO3, was added methyl bromoacetate (0.945 ml, 10 mmole) and stirred at room temperature for 24 hours. The reaction mixture was added to water and extracted with ethyl acetate (3×50 ml), the organic extracts were washed 6× with water, dried (MgSO4) amd evaporated to give the product as a oil.

Aufarbeitung

  1. extractionextracted with ethyl acetate (3×50 ml)
  2. washthe organic extracts were washed 6× with water
  3. dry with materialdried (MgSO4) amd
  4. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-dbc2e752867a4f52ac44b58bf8199368
Quelldatensatz
uspto-grants-2004_02
Patentnummer
US06696566B2

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