HRID364363

反应详情

EQUATION

反应方程式

HRID 364363 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-65 °C

PROCEDURE

实验过程

To a solution of 21.3 ml (0.15 mole) of diisopropyl amine in 300 ml of dry tetrahydrofuran under a continuous nitrogen blanket, at -70° C., was added 61.6 ml of 2.7M n-butyllithium in hexane (0.165 mole) while maintaining the temperature at -60° to -70° C. Subsequent to this addition, the temperature was maintained at -65° C. for approximately 20 minutes. A solution of 20 g (0.12 mole) of 2-chloroquinoline in 60 ml of tetrahydrofuran was added dropwise while maintaining the temperature at -60° to -70° C. After holding the temperature at -65° C. for 20 minutes subsequent to this addition, the entire reaction mixture was poured onto a large excess of dry ice. Most of the solvent was evaporated in a stream of air; the residual solvent was removed by rotary evaporation. The residue was taken up in 300 ml water, made basic with dil aq. sodium hydroxide and washed with 3×50 ml of isopropyl ether. The aqueous layer was filtrate and made acidic (4 to 5 pH) with dilute aqueous hydrochloric acid. The precipitate was collected, washed with water, isopropyl alcohol, and isopropyl ether, and dried, giving 15.4 g (62%) of white crystals, m.p. 190°-210° C. (decomp.). A sample was recrystallized from isopropyl alcohol giving an analytical sample, m.p. 190°-210° C. (decomp.).

WORKUP

后处理

  1. temperaturewhile maintaining the temperature at -60° to -70° C
  2. additionSubsequent to this addition
  3. temperaturewhile maintaining the temperature at -60° to -70° C
  4. customat -65° C.
  5. customfor 20 minutes
  6. additionsubsequent to this addition
  7. customthe entire reaction mixture
  8. customMost of the solvent was evaporated in a stream of air
  9. customthe residual solvent was removed by rotary evaporation
  10. washwashed with 3×50 ml of isopropyl ether
  11. customThe precipitate was collected
  12. washwashed with water, isopropyl alcohol, and isopropyl ether
  13. customdried