HRID1735458

反应详情

EQUATION

反应方程式

HRID 1735458 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

To a solution of 4.48 g of dicyclopropylmethyl alcohol in 20 mL of CH2Cl2 was added 3.6 g of NaN3 followed by 10 g of CCl3CO2H. The resulting mixture was stirred at room temperature for 3 h, diluted with 50 mL of CH2Cl2, washed with NaHCO3 and NaCl solution. Drying over MgSO4 and removal of solvent gave an oil (which was examined by high field 1H NMR and shown to be contaminated by a small amount of ring-opening compound (less than 5%)) which was dissolved in a solution of 7 mL of toluene containing 2.5 g of hexadecyltributyl phosphonium bromide. To the solution was added 5 g of NaBH4 in 15 mL of H2O through a dropping funnel over 30 min. The mixture was stirred at 80° C. for 16 h, layers separated and the organic layer extracted with 10 % HCl. The pH of the aqueous solution was adjusted to 8-9 with NaOH and extracted with ether. After drying over MgSO4, HCl gas was bubbled through the solution and the amine hydrochloride salt which had precipitated was collected by filtration and recrystallized from ether/MeOH to give 1.8 g (35%) of the salt as white crystals, mp 250° C. dec.

WORKUP

后处理

  1. washwashed with NaHCO3 and NaCl solution
  2. dry with materialDrying over MgSO4 and removal of solvent
  3. customgave an oil (which
  4. stirringThe mixture was stirred at 80° C. for 16 h
  5. customlayers separated
  6. extractionthe organic layer extracted with 10 % HCl
  7. extractionextracted with ether
  8. dry with materialAfter drying over MgSO4, HCl gas
  9. customwas bubbled through the solution
  10. customthe amine hydrochloride salt which had precipitated
  11. filtrationwas collected by filtration
  12. customrecrystallized from ether/MeOH