Reaktion #5864

ord-f57d7a6d780c4a4a823cce69c82616b4

Reaktionsgleichung

CC(=O)[O-].[NH4+]
ammonium acetate
COC(=O)C(C=O)N(C=O)C1CCCc2ccccc21
N,α-bis-formyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl) glycine methyl ester
CC(=O)[O-].[NH4+]
ammonium acetate
CC(=O)O
acetic acid
COC(=O)c1cncn1C1CCCc2ccccc21
1-(1,2,3,4-tetrahydronaphthalen-1-yl) -5-imidazolecarboxylic acid methyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturare refluxed for 8 hours
  2. 2
    Extraktionextracted twice, with 100 ml of toluene each time
  3. 3
    Einengenconcentrated
  4. 4
    Sonstigeseparated at silica gel by chromatography

Vorschrift

A mixture of 16.5 g of N,α-bis-formyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl) glycine methyl ester, 65.0 g of ammonium acetate and 100 ml of acetic acid are refluxed for 8 hours. Then additional 50 g ammonium acetate are added and the refluxing is continued for further 4 hours. The solution is diluted with 300 ml of water and extracted twice, with 100 ml of toluene each time. The organic phases are combined, concentrated and separated at silica gel by chromatography. Concentration of the eluate yields 1-(1,2,3,4-tetrahydronaphthalen-1-yl) -5-imidazolecarboxylic acid methyl ester, having a melting point of 63° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246915uspto-grants-1993_09