HRID1072284

反应详情

EQUATION

反应方程式

HRID 1072284 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

A mixture that consists of 54.1 g (100 mmol) of 2,3,4,6-tetra-O-benzyl-mannopyranose, 1.39 g (5 mmol) of tetrabutylammonium chloride and 35.84 g (110 mmol) of cesium carbonate in 500 ml of diethoxymethane is cooled to 0° C. At 0° C., 60.3 g (150 mmol) of 6-bromohexylamine-N-(9-fluorenylmethoxy-carbonyl) is added in drops over 30 minutes while being stirred vigorously. It is stirred for one hour at 0° C. 300 ml of dichloromethane is added, the organic phase is separated, and the aqueous phase is extracted twice with 200 ml of dichloromethane. The solvent of the combined organic phases is distilled off in a vacuum. The residue is taken up in 250 ml of ethanol, and 100 g (1.17 mol) of piperidine is added. It is stirred for five hours at 40° C. The solution is evaporated to the dry state, and the residue is chromatographed on silica gel (mobile solvent: dichloromethane/ethanol/triethylamine=20:2:0.1).

WORKUP

后处理

  1. stirringIt is stirred for one hour at 0° C
  2. customthe organic phase is separated
  3. extractionthe aqueous phase is extracted twice with 200 ml of dichloromethane
  4. distillationThe solvent of the combined organic phases is distilled off in a vacuum
  5. stirringIt is stirred for five hours at 40° C
  6. customThe solution is evaporated to the dry state
  7. customthe residue is chromatographed on silica gel (mobile solvent: dichloromethane/ethanol/triethylamine=20:2:0.1)