反应详情

温度

80 °C

(2R,3R,4R)-3,4-Dibenzyloxy-2-benzyloxymethylpyrrolidine (Compound 1) (0.25 g, 0.62 mmol) was dissolved in methyl-isobutylketone (15 ml). Potassium carbonate (0.17 g, 1.2 mmol) and potassium iodide (0.03 g, 0.18 mol) was added. After stirring for 10 min at 25° C. cyclopropylmethylbromide (0.078 ml, 0.81 mmol) was added. The mixture was stirred under a N2 atmosphere at 80° C. for 24 hours and evaporated in vacuo. Water (20 ml) was added and extraction with methylene chloride (3×20 ml), drying of the organic phases with magnesium sulphate and evaporation of the solvent in vacuo afforded a yellow oil. Purification of the crude product twice on a silica gel column (1: Eluent: CH2Cl2/MeOH (19:1) and 2: Eluent: CH2Cl2/MeOH (39:1)) gave (2R,3R,4R)-3,4-dibenzyloxy-2-benzyloxymethyl-1-cyclopropylmethylpyrrolidine (0.213 g, yield: 75%) as an oil.

1. additionwas added
2. customevaporated in vacuo
3. additionWater (20 ml) was added
4. extractionextraction with methylene chloride (3×20 ml)
5. dry with materialdrying of the organic phases with magnesium sulphate and evaporation of the solvent in vacuo
6. customafforded a yellow oil
7. customPurification of the crude product twice on a silica gel column (1: Eluent: CH2Cl2/MeOH (19:1) and 2: Eluent: CH2Cl2/MeOH (39:1))