HRID1060415

反应详情

EQUATION

反应方程式

HRID 1060415 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

N-(2,6-Dichlorobenzoyl)-4-(2,6-dimethoxyphenyl)-L-phenylalanine, ethyl ester (0.16 g, prepared in a fashion similar to that of the methyl ester described in Example 8) was dissolved in anhydrous CH2Cl2 (8 mL). The solution was cooled to −78° C. and BBr3 (0.56 mL, 1 M solution in CH2Cl2) was added. The mixture was allowed to warm to 0° C., and stirred at that temperature for 2 h. The mixture was subsequently warmed to room temperature and quenched with satd. NaHCO3 (5 mL). The mixture was stirred for 1 h, and diluted with CH2Cl2. The organic phase was dried (MgSO4) and concentrated. The residue was purified by flash column chromatography (silica gel; eluent: EtOAc/hexanes 1:2) to give 40 mg of N-(2,6-dichlorobenzoyl)-4-(2-hydroxy-6-methoxyphenyl)-L-phenylalanine ethyl ester. ESMS: m/z 488 (MH+).

WORKUP

后处理

  1. temperatureto warm to 0° C.
  2. temperatureThe mixture was subsequently warmed to room temperature
  3. customquenched with satd
  4. stirringThe mixture was stirred for 1 h
  5. additiondiluted with CH2Cl2
  6. dry with materialThe organic phase was dried (MgSO4)
  7. concentrationconcentrated
  8. customThe residue was purified by flash column chromatography (silica gel; eluent: EtOAc/hexanes 1:2)