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

HRID 1375588Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1375588
[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) and 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)
  4. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-f11cfb1394de4bf6b44418da7e9af3b6
Quelldatensatz
uspto-grants-2007_01
Patentnummer
US07169794B2

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