反应详情

6.95 g (44 mmol) of powdered potassium permanganate dissolved in a mixture of 100 ml of water and 100 ml of glacial acetic acid as well as 0.73 g (2 mmol) of tetrabutylammonium iodide were added to a solution of 5.0 g (10.83 mmol) of tert-butyl (3RS,4RS)-4-[4-(2-hydroxy-ethyl)-phenyl]-3-naphthalen-2-ylmethoxy-piperidine-1-carboxylate in 500 ml of benzene. The reaction mixture was stirred intensively for 48 hours. For the working-up, the phases were separated. The organic phase was washed with 100 ml of saturated sodium thiosulphate solution. The aqueous phase was decolorized by the addition of saturated sodium thiosulphate solution and subsequently extracted twice with 100 ml of ethyl acetate and 100 ml of methylene chloride each time. The organic phases were combined, dried over sodium sulphate and evaporated under reduced pressure. For purification, the crude material was chromatographed on silica gel using a 9:1 mixture of methylene chloride and methanol as the eluent after the column had previously been prepared with a 90:10:0.1 mixture of methylene chloride, methanol and ammonia. There were obtained 2.6 g (50% of theory) of (3RS,4RS)-[4-(1-tert-butoxycarbonyl-3-naphthalen-2-ylmethoxy-piperidin-4-yl)-phenyl]-acetic acid as a colourless, amorphous solid; MS: 476 (M+H)+.

1. customthe phases were separated
2. washThe organic phase was washed with 100 ml of saturated sodium thiosulphate solution
3. additionThe aqueous phase was decolorized by the addition of saturated sodium thiosulphate solution
4. extractionsubsequently extracted twice with 100 ml of ethyl acetate and 100 ml of methylene chloride each time
5. dry with materialdried over sodium sulphate
6. customevaporated under reduced pressure
7. customFor purification
8. customthe crude material was chromatographed on silica gel using
9. additiona 9:1 mixture of methylene chloride and methanol as the eluent after the column
10. customhad previously been prepared with a 90:10:0.1 mixture of methylene chloride, methanol and ammonia