HRID35366

反应详情

EQUATION

反应方程式

HRID 35366 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a suspension of 2.1 g of lithium aluminum hydride in 200 ml of tetrahydrofuran was added 6.06 g of trans-4a,5,6,11b-tetrahydro-4-isopropyl-10-fluoro-2H-[1]benzoxepino[5,4-b]-1,4-oxazin-3(4H)-one in portions and the mixture was then refluxed for about one hour. The mixture was then cooled in ice, decomposed by the addition of 6 ml of 10% aqueous sodium hydroxide solution, and stirred for 16 hours. The solids present in the reaction mixture were separated by filtration and washed with water and the solvent was evaporated from the filtrate to leave a residual oil. The oil was dissolved in ether and a solution of methanesulfonic acid in ether was added until no more cloudiness occurred on addition. The solid was then separated by filtration and triturated in ether to give a tacky solid. This solid was recrystallized from a mixture of methanol and ethyl acetate to give trans-10-fluoro-4-isopropyl-3,4,4a,5,6,11b-hexahydro-2H-[1]benzoxepino[5,4-b]-1,4-oxazine methanesulfonate melting at about 163°-165° C.

WORKUP

后处理

  1. temperaturethe mixture was then refluxed for about one hour
  2. temperatureThe mixture was then cooled in ice
  3. customThe solids present in the reaction mixture were separated by filtration
  4. washwashed with water
  5. customthe solvent was evaporated from the filtrate
  6. customto leave a residual oil
  7. additionoccurred on addition
  8. customThe solid was then separated by filtration
  9. customtriturated in ether
  10. customto give a tacky solid
  11. customThis solid was recrystallized from a mixture of methanol and ethyl acetate