Reacción #77591

Ecuación de reacción

3-nitro-5-methoxycarbonylbenzoic acid

water

potassium carbonate

→

title compound

Rendimiento 93.6%

Methyl 3-Amino-5-hydroxymethylbenzoate

Rendimiento 93.6%

Disolventes

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONwas added
2. 2
   Temperaturacooling
3. 3
   workup.STIRRINGAfter stirring for 18 hours
4. 4
   ExtracciónIt was extracted with ethyl acetate, and theorganic layer
5. 5
   Lavadowas washed with salt solution
6. 6
   SecadoAfter drying with magnesium sulfate
7. 7
   workup.DISSOLUTIONthe resulting solid was dissolved in 800 ml of ethyl acetate
8. 8
   workup.ADDITION750 mg of 10% Pd/C was added
9. 9
   workup.STIRRINGstirring
10. 10
    Filtraciónit was subjected to the filtration
11. 11
    Concentraciónthe filtrate was concentrated

Procedimiento

85 g of 3-nitro-5-methoxycarbonylbenzoic acid was dissolved in 200 ml of THF under a flow of nitrogen, and 43.4 ml of borane dimethylsulfide complex was added with stirring under ice-cooling. After stirring for 18 hours, 200 ml of water was added, and then 96 g of potassium carbonate was added. It was extracted with ethyl acetate, and theorganic layer was washed with salt solution. After drying with magnesium sulfate, the resulting solid was dissolved in 800 ml of ethyl acetate, 750 mg of 10% Pd/C was added, and stirring was continued under the flow of hydrogen. After the reaction was completed, it was subjected to the filtration, and then the filtrate was concentrated to produce 64 g of the title compound.

Fuente