反应详情

2.75 g of 2-aminopropan-1,3-diol and 5.9 g of 1-benzyl-4-piperidone are dissolved in 60 ml of methylene chloride and while cooling with ice a total of 9.9 g of sodium triacetoxyborohydride are added batchwise. The mixture is left to stand overnight at ambient temperature. 60 ml of methylene chloride and some water are added, then conc. hydrochloric acid is added while cooling with ice until an acid reaction is obtained. The mixture is stirred for about another 15 min. with cooling and then made clearly alkaline with 4 N sodium hydroxide solution. The aqueous phase is separated off, the organic phase is washed with a very little water, dried over sodium sulphate and freed from solvent in vacuo. 8 g of substance are obtained which are chromatographed with methylene chloride/methanol 8:2 over 150 g of silica gel. The uniform fractions according to TLC are combined and freed from solvent in vacuo. 7.3 g of 1-benzyl-4-(1,3-dihydroxyprop-2-ylamino)-piperidine are obtained.

1. additionare added batchwise
2. waitThe mixture is left
3. temperaturewhile cooling with ice until an acid reaction
4. customis obtained
5. temperaturewith cooling
6. customThe aqueous phase is separated off
7. washthe organic phase is washed with a very little water
8. dry with materialdried over sodium sulphate
9. custom8 g of substance are obtained which
10. customare chromatographed with methylene chloride/methanol 8:2 over 150 g of silica gel