反应详情

A degassed solution, under nitrogen, of 3.70 g of (3aS-cis)-5-ethoxy-1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indole in 50 ml of dry chloroform was treated with 2.00 g of nitronium tetrafluoroborate at a reaction temperature of +10°. After 20 minutes, the reaction was quenched by the addition of ice and saturated sodium bicarbonate solution with vigorous stirring. The organic layer was separated, dried over anhydrous sodium sulfate and concentrated to an oil. This was purified by chromatography over silica gel using ethyl acetate as the eluent. The fractions containing the product were combined and concentrated to an oil which crystallized from hexane to afford crystals of pure (3aS-cis)-5-ethoxy-1,2,3,3a,8,8a-hexahydro-7-nitro-1,3a, 8-trimethylpyrrolo[2,3-b]indole, mp 106°-108° C. ANALYSIS: Calculated for C15H21N3O2 : 61.84%C 7.27%H 14.44%N Found: 61.88%C 7.26%H 14.35%N

1. customthe reaction was quenched by the addition of ice and saturated sodium bicarbonate solution with vigorous stirring
2. customThe organic layer was separated
3. dry with materialdried over anhydrous sodium sulfate
4. concentrationconcentrated to an oil
5. customThis was purified by chromatography over silica gel
6. additionThe fractions containing the product
7. concentrationconcentrated to an oil which
8. customcrystallized from hexane