Reacción #2066840

ord-a134b7b10f5347c1a934a6c3b6241602

Ecuación de reacción

Cc1cccc2ccccc12
1-methylnaphthalene
CCCCOP(=O)(OCCCC)OCCCC
tributylphosphate
O=Cc1cccc2ccccc12
1-naphthaldehyde
Rendimiento 25.7%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe same reaction
  2. 2
    OtroThe organic material isolated from this run
  3. 3
    Lavadowas eluted with a solution of 5% ether in petroleum ether (bp=60°-80° C.)

Procedimiento

The same reaction was tried in a modified cell, without the crank 23. 2 g (14 mmol) of 1-methylnaphthalene in 3 g of tributylphosphate was allowed to react for 40 hours with electrochemically produced Co(III) sulphate at 40°-45° C. The electrolyte solution was composed of 0.12M Co(II) sulphate in 2M H2SO4. The current was 200 mA. The organic material isolated from this run was placed on a silica gel column, which was eluted with a solution of 5% ether in petroleum ether (bp=60°-80° C.). The initial band consisted of 860 mg (6 mmol, 43%) of starting material. The second band yielded 447 mg (2.9 mmol) of 1-naphthaldehyde. The aldehyde yield was 36% based on consumed starting material. The aldehyde yield was 36% based on consumed starting material. The infrared spectrum of the product was identical to that of an authentic sample.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04482438uspto-grants-1984_11