HRID2224640

反应详情

EQUATION

反应方程式

HRID 2224640 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-70 °C

PROCEDURE

实验过程

The following reaction was performed under a N2 atmosphere. A mixture of N-(4-bromophenyl)-2-benzothiazolamine (0.492 mol) in THF (2700 ml) was stirred at −70° C. Butyllithium (0.984 mol; 2.5 M in hexane) was added dropwise at −65° C. The mixture was stirred for one hour. A solution of 2-ethyl-butanal (0.492 mol) in THF (300 ml) was added dropwise at −75° C. The mixture was allowed to warm to RT overnight. A 10% aqueous NH4Cl solution (3000 ml) was added and the mixture was stirred for 15 minutes. The separated aqueous phase was extracted with EtOAc (1000 ml). The separated organic layer was dried, filtered and the solvent evaporated. The residue was crystallized from methyl isobutyl keton. The precipitate was filtered off and dried, yielding 109 g (68%) of (±)-4-(2-benzothiazolylamino)-α-(1-ethyl-propyl)benzenemethanol (interm 28).

WORKUP

后处理

  1. customThe following reaction
  2. stirringThe mixture was stirred for one hour
  3. temperatureto warm to RT overnight
  4. stirringthe mixture was stirred for 15 minutes
  5. extractionThe separated aqueous phase was extracted with EtOAc (1000 ml)
  6. customThe separated organic layer was dried
  7. filtrationfiltered
  8. customthe solvent evaporated
  9. customThe residue was crystallized from methyl isobutyl keton
  10. filtrationThe precipitate was filtered off
  11. customdried