HRID615261

反应详情

EQUATION

反应方程式

HRID 615261 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
25 °C

PROCEDURE

实验过程

To a stirred mixture of 3,3-dimethoxybutan-2-one (J.Chem.Soc. 1953, 3135; 1.32 g., 10 m moles) and ammonium acetate (7.7 g., 0.1 mole) in methanol (30 ml.) at 25° C. was added sodium cyanoborohydride (380 mg., 6 m moles) and the pH of the mixture was reduced to 6.0 by addition of a solution of HCl in methanol. The mixture was stirred for 2 hours at 25° C. then the solvent was evaporated under reduced pressure. The residue was taken up in water and the pH adjusted to 5 with 2N aqueous HCl. The solution was washed with ether (3×20 ml.) and the pH of the aqueous phase raised to above 10 by addition of sodium carbonate. The product was extracted with ether (5×20 ml.) and the combined extracts were dried (MgSO4) and evaporated to dryness to give 1-methyl-2,2-dimethoxypropylamine (1.02 g., 77%) as a pale yellow oil having the following n.m.r. spectrum in CDCl3 : 1.05 (d, 3H); 1.2 (s, 3H); 1.6 (m, 2H); 3.25 (s, 6H); 3.0-3.6 (m, 1H).

WORKUP

后处理

  1. customthe solvent was evaporated under reduced pressure
  2. washThe solution was washed with ether (3×20 ml.)
  3. temperaturethe pH of the aqueous phase raised to above 10 by addition of sodium carbonate
  4. extractionThe product was extracted with ether (5×20 ml.)
  5. dry with materialthe combined extracts were dried (MgSO4)
  6. customevaporated to dryness