HRID1058331

反应详情

EQUATION

反应方程式

HRID 1058331 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of 78.0 g (0.312 mol) 2-azidomethylphenylacetic acid t-butyl ester in 1.36 L THF was added 7.8 g (50% water wet) 5% Pd on C and the mixture shaken mechanically in a 2 L heavy-walled flask under H2 at 45 psi for 2 h. The catalyst was removed by filtration through a bed of celite, rinsing with 250 mL THF. To the filtrate was added a solution of 31.25 g (0.347 mol) oxalic acid in 500 mL methyl tert-butyl ether, and the resultant suspension stirred at room temperature for 30 min. The solid was collected on a filter and washed with 300 mL methyl tert-butyl ether (the filtration was very slow, requiring about 3 hours). Drying under reduced pressure at 60° C. for 18 h gave 42.4 g (39% overall from 2-bromomethylphenylacetic acid) tert-butyl [2-(aminomethyl)phenyl]acetate oxalate salt as a white powder. The product is unstable as the free base, and will cyclize to the amide over several hours at room temperature.

WORKUP

后处理

  1. customThe catalyst was removed by filtration through a bed of celite
  2. washrinsing with 250 mL THF
  3. customThe solid was collected on
  4. filtrationa filter
  5. washwashed with 300 mL methyl tert-butyl ether (
  6. filtrationthe filtration
  7. waitrequiring about 3 hours
  8. customDrying under reduced pressure at 60° C. for 18 h