Reacción #58478

ord-9274e00d4d174b7d9c1bd6c9718ddb6b

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThen the organic solution was separated
  2. 2
    Lavadothe salts were washed twice with benzene
  3. 3
    Secadodried over sodium sulfate
  4. 4
    Concentraciónconcentrated in vacuo

Procedimiento

To a stirred solution of 3.9 g (60 mmol) KCN in 5.5 ml of water at 4° C., a solution of 2.9 g (20 mmol) of 4-oxo-tetrahydro furane 3-carboxylic acid methyl ester in ether (26 ml) was added. To the precipitate of salts, 3.5 ml H2SO4 (18 N) was added and stirred for 16 hours. Then the organic solution was separated, the salts were washed twice with benzene, dried over sodium sulfate and concentrated in vacuo to give 4-cyano-tetrahydro furane 3-carboxylic acid methyl ester.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07423057B2uspto-grants-2008_09