Reacción #52570

Ecuación de reacción

4-methanesulfonyl-2-nitrobenzoyl chloride

potassium cyanide

4-methylene-3-oxabicyclo[3.2.1]octan-2-one

triethylamine

potassium cyanide

4-methanesulfonyl-2-nitro-benzoic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester

→

4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one

Disolventes

ethyl acetate

acetonitrile

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGstirring
2. 2
   workup.WAITis continued for a further 2 hours until conversion
3. 3
   Extracciónextracted at a pH value of 13 against water
4. 4
   Extracciónextracted at a pH value of approximately 4
5. 5
   Secadodried over Na2SO4
6. 6
   Concentraciónconcentrated to a slight extent
7. 7
   workup.DISSOLUTIONThe product, dissolved in warm ethyl acetate
8. 8
   workup.ADDITIONis treated with activated carbon
9. 9
   Filtraciónfiltered off with suction (suction filter) through a small amount of silica gel
10. 10
    Concentraciónconcentrated further
11. 11
    Otroto crystallise
12. 12
    workup.ADDITIONby adding a small amount of hexane

Procedimiento

2.76 g (0.02 mol) of 93% 4-methylene-3-oxabicyclo[3.2.1]octan-2-one and 4.45 g (0.044 mmol) of triethylamine are stirred for 7 hours at room temperature in 50 ml of acetonitrile in the presence of 130 mg (2 mmol) of potassium cyanide. 4.22 g (0.16 mol) of freshly prepared 4-methanesulfonyl-2-nitrobenzoyl chloride are then introduced and stirring is carried out for 12 hours at a temperature of 20° C. If, according to monitoring by thin-layer chromatography, relatively large amounts of the intermediate 4-methanesulfonyl-2-nitro-benzoic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester (known from U.S. Pat. No. 5,801,120) are still detectable, then a further 130 mg (2 mmol) of potassium cyanide are added and stirring is continued for a further 2 hours until conversion is complete. The reaction mixture is then taken up in ethyl acetate and extracted at a pH value of 13 against water. The aqueous phase is then acidified using hydrochloric acid and extracted at a pH value of approximately 4 using fresh ethyl acetate, dried over Na2SO4 and concentrated to a slight extent. The product, dissolved in warm ethyl acetate, is treated with activated carbon and filtered off with suction (suction filter) through a small amount of silica gel, then concentrated further and caused to crystallise by adding a small amount of hexane. 1.69 g of pure 4-hydroxy-3-(4-methanesulfonyl-2-nitrobenzoyl)-bicyclo[3.2.1]oct-3-en-2-one having a melting point of 170-170.5° C. are obtained. Further product (1.65 g) can be obtained from the mother liquor by recrystallisation. Total yield: 3.34 g, or 49.1% based on the starting material 4-methylene-3-oxabicyclo[3.2.1]octan-2-one used or 57.1% based on the starting material 4-methanesulfonyl-2-nitrobenzoic acid used. 1H-NMR (CDCl3): 15.94 ppm, s, 1H; 8.74, s, 1H; 8.24 ppm, d, 1H; 7.48 ppm, d, 1H; 3.20 ppm, m, 1H; 3.19 ppm, s, 3H; 2.84 ppm, m, 1H; 2.0-2.3 ppm, 4H; 1.6-1.8 ppm, 2H.

Fuente