HRID330494

反应详情

EQUATION

反应方程式

HRID 330494 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A mixture of 7.5 g of phenylguanidine hydrogen carbonate and 7.4 g of methoxyacetylacetone is heated at 100° C. for four hours with stirring, the evolution of carbon dioxide which occurs subsiding as the reaction progresses. After the brown emulsion has been cooled to room temperature, 60 ml of diethyl ether are added and the whole is then washed three times with 20 ml of water each time, dried over sodium sulphate and filtered, and the solvent is evaporated. The 10.5 g of oily residue are dissolved in 140 ml of diethyl ether, and then 4.4 g of 65% nitric acid are added thereto with stirring. The suspension of the resulting nitrate salt is stirred for a further 20 minutes and is then filtered and washed with 100 ml of diethyl ether. 6 g of 30% sodium hydroxide solutions are added with stirring to a mixture consisting of 11 g of the nitrate sale, 80 ml of diethyl ether and 60 ml of water, the organic phase is separated off, washed twice with 40 ml of water each time, dried over sodium sulfate and filtered, and the solvent is evaporated. The 8.7 g of light-brown oily residue are crystallised with 100 ml of petroleum ether (b.p. 50°-70° C.), filtered and dried. The 8 g of pale, beige-coloured crystalline powder melt at 59°-60° C.; yield: 92% of the theoretical yield, relative to phenylguanidine hydrogen carbonate.

WORKUP

后处理

  1. customas the reaction progresses
  2. temperatureAfter the brown emulsion has been cooled to room temperature
  3. washthe whole is then washed three times with 20 ml of water each time
  4. dry with materialdried over sodium sulphate
  5. filtrationfiltered
  6. customthe solvent is evaporated
  7. dissolutionThe 10.5 g of oily residue are dissolved in 140 ml of diethyl ether
  8. addition4.4 g of 65% nitric acid are added
  9. stirringwith stirring
  10. additionThe suspension of the resulting nitrate salt
  11. stirringis stirred for a further 20 minutes
  12. filtrationis then filtered
  13. washwashed with 100 ml of diethyl ether
  14. addition6 g of 30% sodium hydroxide solutions are added
  15. stirringwith stirring to a mixture
  16. customthe organic phase is separated off
  17. washwashed twice with 40 ml of water each time
  18. dry with materialdried over sodium sulfate
  19. filtrationfiltered
  20. customthe solvent is evaporated
  21. customThe 8.7 g of light-brown oily residue are crystallised with 100 ml of petroleum ether (b.p. 50°-70° C.)
  22. filtrationfiltered
  23. customdried
  24. custommelt at 59°-60° C.