Reacción #1687627

ord-d0fd52035f454e118ab995b215846694

Ecuación de reacción

CCOC(C)=O
ethyl acetate
C=[N+]=[N-]
diazomethane
c1cncc(-c2c[nH]nn2)c1
68
c1cncc(-c2c[nH]nn2)c1
4-(3-Pyridyl)-1,2,3-triazole
CC(=O)O
acetic acid
Cn1ncc(-c2cccnc2)n1
2-Methyl-4-(3-pyridyl)-1,2,3,-triazole

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe mixture was evaporated in vacuo
  2. 2
    workup.ADDITIONWater (75 ml) was added
  3. 3
    ExtracciónExtraction with 3×100 ml of ether
  4. 4
    Secadodrying of the organic phase over magnesium sulphate, and removal of the solvent in vacuo
  5. 5
    Otrogave a brown solid which
  6. 6
    Otrogiving a colorless solid, 69

Procedimiento

A solution of ca. 3.0 g (0.070 mol) diazomethane in ether was added dropwise to a solution of 6.0 g (0.04 mol) of 68 in 150 ml of ethanol at room temperature. The solution was stirred overnight at ambient temperature. Ca. 1 ml of acetic acid was added and the mixture was evaporated in vacuo. Water (75 ml) was added and the solution made basic with ammonia. Extraction with 3×100 ml of ether, drying of the organic phase over magnesium sulphate, and removal of the solvent in vacuo gave a brown solid which as applied to a silica gel column (eluent: ethyl acetate) giving a colorless solid, 69. Yield: 2.8 g (0.018 mol, 43%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE036374uspto-grants-1999_11