HRID217936

反应详情

EQUATION

反应方程式

HRID 217936 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
63 °C

PROCEDURE

实验过程

[4-(4-Hydroxyphenyl)butyl]carbamic acid tert-butyl ester (38 g, 0.143 mole), cesium carbonate (84 g, 0.257 mole), and (2-bromoethyl)carbamic acid benzyl ester 14 (59 g, 0.23 mole) were combined in DMF (200 ml). The mixture was mechanically stirred under nitrogen at 63° C. for 5.5 h, and allowed to stand at room temperature overnight. An additional amount of (2-bromoethyl)carbamic acid benzyl ester 14 (5 g, 0.019 mole) and cesium carbonate (7.1 g, 0.21 mole) were added, and the reaction was further stirred at 65° C. for 1 h. Toluene was then added, and the stirring mixture was allowed to cool to room temperature. The mixture was suction filtered through a medium sintered glass buchner funnel and washed with toluene. The solvents were removed under vacuum at 75° C. The remaining oil was washed with hexanes (2×400 mL), then dissolved in ether (500 ml) and washed with a mixture of water and brine (10:1, 4×100 mL). The remaining solution was suction filtered through a 30 g pad of silica gel and the solvent evaporated. The residue was washed with hexanes (3×400 ml), and then placed under vacuum for 2 h to afford 61.8 g of the product 15 which was used without further purification. 1H NMR (300 MHz, CDCl3) δ 1.45 (s, 9H), 1.54 (m, 4H), 2.56 (t, 2H), 3.20 (m, 2H), 3.50 (m, 2H), 3.98 (t, 2H), 4.75 (br s, 1H), 5.00 (br s, 1H), 5.09 (s, 2H), 6.80 (d, 2H), 7.06 (d, 2H), 7.34 (m, 5H).

WORKUP

后处理

  1. waitto stand at room temperature overnight
  2. stirringthe reaction was further stirred at 65° C. for 1 h
  3. temperatureto cool to room temperature
  4. filtrationfiltered through a medium sintered glass buchner funnel
  5. washwashed with toluene
  6. customThe solvents were removed under vacuum at 75° C
  7. washThe remaining oil was washed with hexanes (2×400 mL)
  8. dissolutiondissolved in ether (500 ml)
  9. washwashed with a mixture of water and brine (10:1, 4×100 mL)
  10. filtrationfiltered through a 30 g pad of silica gel
  11. customthe solvent evaporated
  12. washThe residue was washed with hexanes (3×400 ml)
  13. waitplaced under vacuum for 2 h