HRID411931

反应详情

EQUATION

反应方程式

HRID 411931 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Dry tetrahydrofuran (300 ml) was added to a mixture of methyltriphenylphosphonium iodide (17.00 g, 42.0 mmoles) and potassium t-butoxide (4.72 g, 42.0 mmoles) and stirred at room temperature for 10 minutes. 3,5-bis(3′,5′-di-t-butylstyryl)benzaldehyde (17.00 g, 42.0 mmoles) was then added and the reaction mixture was stirred at room temperature for 75 minutes. The solvent was then evaporated and the remaining sludge was triturated with dichloromethane-pet.ether (40-60) (1:9) and filtered through silica, rinsing thoroughly with the same solvent mixture. The solvent was evaporated to give 3,5-bis(3′,5′-di-t-butylstyryl)styrene (14.83 g, 99%), mp 150° C. (Found: C, 90.03; H, 9.98. C40H52 requires C, 90.16; H, 9.84%); λmax(CHCl3)/nm 318 (ε/dm3 mol-1 cm-1 68500); δH(500 MHz; CDCl3) 1.39 (36H, s, tBu), 5.34 (1H, d, J 11, 8-H), 5.88 (1H, d, J 18, 8-H), 6.79 (1H, dd, J 11 and 18, 7-H), 7.15 (2H, d, J 16, 7′-H), 7.25 (2H, d, J 16, 8′-H), 7.38 (2H, t, J 1.75, 1′-H), 7.42 (4H, d, J 1.75, 3′, 5′-H), 7.49 (2H, d, J 1.3, 3,5-H), 7.63 (1H, m, 1-H).

WORKUP

后处理

  1. stirringthe reaction mixture was stirred at room temperature for 75 minutes
  2. customThe solvent was then evaporated
  3. customthe remaining sludge was triturated with dichloromethane-pet
  4. filtrationether (40-60) (1:9) and filtered through silica
  5. washrinsing thoroughly with the same solvent mixture
  6. customThe solvent was evaporated