HRID11066

反应详情

EQUATION

反应方程式

HRID 11066 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 2,6-dichlorotoluene (20.1 g, 0.125 mol), N-bromosuccinimide (24.6 g, 0.138 mol) and 2,2′-azobisisobutyronitrile (0.41 g, 2.50 mmol) in dry benzene (300 mL) under N2 was stirred at reflux for 6 h with continuous irradiation from a 100W lamp. The resulting reaction mixture was concentrated under vacuum (to 50 mL), cooled and filtered, washing with dry benzene. The filtrate (containing the crude benzyl bromide) was treated directly with triphenylphosphine (49.3 g, 0.188 mol), stirring at reflux for 17 h. After cooling, the precipitate was collected by filtration, washing thoroughly with dry benzene, then pentane, and dried under vacuum at 50° C. to give the phosphonium salt (511) as a cream powder (62.1 g, 99%), mp (benzene) 247–250° C. 1H NMR (CDCl3) δ 7.76 (m, 9H), 7.64 (m, 6H), 7.18 (s, 3H), 5.50 (d, J=14.3 Hz, 2H). Found: C, 60.03; H, 3.76. C25H2,BRCl2P requires C, 59.79; H, 4.01.

WORKUP

后处理

  1. customThe resulting reaction mixture
  2. concentrationwas concentrated under vacuum (to 50 mL)
  3. temperaturecooled
  4. filtrationfiltered
  5. washwashing with dry benzene
  6. additionThe filtrate (containing the crude benzyl bromide)
  7. stirringstirring
  8. temperatureat reflux for 17 h
  9. temperatureAfter cooling
  10. filtrationthe precipitate was collected by filtration
  11. washwashing thoroughly with dry benzene
  12. dry with materialpentane, and dried under vacuum at 50° C.