HRID1251514

反应详情

EQUATION

反应方程式

HRID 1251514 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

4-Acetoxy-3,5-di-tert-butylbenzaldehyde (113.16 g, 0.41 mol) was placed in a 2 L round-bottomed flask fitted with a magnetic stirrer. Benzene (500 mL) was added and the mixture was stirred until the solids dissolved. To the resulting red solution was added iert-butylhydroxylamine (43.80 g, 0.49 mol) and silica gel (20 g). The mixture was refluxed overnight at which time TLC showed no remaining startin material (Rf=0.31 for product and 0.80 for starting material using 3:1 hexanes/EtOAc). The benzene was removed in vacuo on a rotovap to provide a grey solid. The solid was dissolved in a minimum amount of ethyl acetate and the flask was left to stand in the freezer. The white crystals which formed were separated, washed with hexanes and dried under vacuum to afford 105.78 g of the title compound as a crystalline white solid (74.4% yield), m.p. 227.0-248.9° C.

WORKUP

后处理

  1. customfitted with a magnetic stirrer
  2. dissolutiondissolved
  3. temperatureThe mixture was refluxed overnight at which time TLC
  4. customThe benzene was removed in vacuo on a rotovap
  5. customto provide a grey solid
  6. waitthe flask was left
  7. customThe white crystals which formed
  8. customwere separated
  9. washwashed with hexanes
  10. customdried under vacuum