Reaktion #53318

ord-ed78377417f44c5a83a9eb9571d4c6de

Reaktionsgleichung

CCOC(=O)CN.Cl
glycine ethyl ester hydrochloride
CCOC(CBr)OCC
bromoacetaldehyde diethyl acetal
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
[I-].[Na+]
sodium iodide
Cl
hydrochloric acid
CCOC(=O)CNCC(OCC)OCC
title compound
CCOC(=O)CNCC(OCC)OCC
ethyl 2-[(2,2-diethoxyethyl)amino]acetate

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with ethyl acetate
  2. 2
    Extraktionextracted with methylene chloride
  3. 3
    TrocknenThe organic layer was dried over anhydrous sodium sulfate
  4. 4
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure

Vorschrift

To a suspension of the glycine ethyl ester hydrochloride (1.00 g) and bromoacetaldehyde diethyl acetal (1.08 ml) in N,N-dimethylformamide (30 ml), were added cesium carbonate (4.67 g) and sodium iodide (107 mg) and the mixture was stirred at 100° C. for 4 hours. The reaction mixture was adjusted to pH 2 with 1N hydrochloric acid and washed with ethyl acetate. The aqueous layer was adjusted to pH 11 with 1N aqueous solution of sodium hydroxide and extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate and thereafter the solvent was distilled off under reduced pressure to obtain the title compound (860 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06858599B2uspto-grants-2005_02