Reacción #49802

Ecuación de reacción

{o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}acetyl chloride

N-methyl-N-nitroso-p-toluenesulfonamide

potassium hydroxide

→

title product

1-Diazo-3-{o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}-2-propanone

Disolventes

tetrahydrofuran

ether

methanol

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.DISTILLATIONThe diazomethane is distilled over,
2. 2
   Otrocondensed with a dry ice/acetone condenser
3. 3
   Otrocollected
4. 4
   workup.STIRRINGstirred for 30 minutes
5. 5
   Concentraciónconcentrated in vacuo

Procedimiento

A mixture of potassium hydroxide in methanol (20.0 mL of a 4M solution ) is heated to 42° C. and treated dropwise with a mixture of N-methyl-N-nitroso-p-toluenesulfonamide (4 g, 18.7 mmol) in ether (40 mL). The diazomethane is distilled over, condensed with a dry ice/acetone condenser and collected. The diazomethane/ether solution is stirred in an ice-bath, treated dropwise with a solution of {o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}acetyl chloride (1.09 g, 2.32 mmol) in tetrahydrofuran, stirred for 30 minutes and concentrated in vacuo to give the title product as a yellow oil which is identified by NMR spectral analyses.

Fuente