HRID1459650

反应详情

EQUATION

反应方程式

HRID 1459650 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

(2R,3R,4R)-3,4-Dibenzyloxy-2-benzyloxymethyl-1-(2-phthal-imidoethyl)pyrrolidine (Compound 19) (0.64 g, 1.1mmol) was dissolved in ethanol (20 ml) and hydrazin, hydrate (0.215 ml, 4.4 mmol) was added. The clear solution was stirred for 4 hours at 40° C. and for 18 hours at room temperature. The white precipitate was filtered off and the filtrate evaporated in vacuo. The residue was partitioned between aqueous hydrochloric acid and methylene chloride. The water phase adjusted to pH 11with 2N sodium hydroxide and extracted with methylene chloride (2×100 ml) and with diethylether (100 ml). Drying of the combined organic phases with magnesium sulphate and evaporation of the solvent in vacuo afforded the crude product as an oil. Purification on silica gel (Eluent: Ethyl acetate) gave (2R,3R,4R)-1-(2-aminoethyl)-3,4-dibenzyloxy-2-benzyloxymethylpyrrolidine (0.015 g) as an oil.

WORKUP

后处理

  1. filtrationThe white precipitate was filtered off
  2. customthe filtrate evaporated in vacuo
  3. customThe residue was partitioned between aqueous hydrochloric acid and methylene chloride
  4. extractionextracted with methylene chloride (2×100 ml) and with diethylether (100 ml)
  5. dry with materialDrying of the combined organic phases with magnesium sulphate and evaporation of the solvent in vacuo
  6. customafforded the crude product as an oil
  7. customPurification on silica gel (Eluent: Ethyl acetate)