反应 #1435689

ord-8b933451f4304ad18c733eccc056d0ed

反应方程式

CC(Br)C(=O)Cl
2-bromopropionic acid chloride
Cc1ccc(S(=O)(=O)O)cc1.NCCC(=O)OCc1ccccc1
β-alanine-benzyl ester-p-toluenesulfonic acid salt
CCN(CC)CC
triethylamine
Cl
hydrochloric acid
CC(Br)C(=O)NCCC(=O)OCc1ccccc1
2-Bromopropionyl-β-alanine-benzyl ester

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他to exceed 5° C
  2. 2
    workup.ADDITIONAfter addition
  3. 3
    workup.WAITfor 2 hours at room temperature
  4. 4
    其他The organic phase is separated
  5. 5
    洗涤washed once each with 300 ml of 5% aqueous hydrochloric acid, 300 ml of 5% aqueous soda solution and 400 ml of water
  6. 6
    其他The organic phase is dried on magnesium sulfate
  7. 7
    其他evaporated to dryness in a vacuum
  8. 8
    其他The residue recrystallizes from diisopropyl ether

实验过程

53.65 g (313 mmol) of 2-bromopropionic acid chloride is added in drops at 0° C. to 100 g (285 mmol) of β-alanine-benzyl ester-p-toluenesulfonic acid salt and 31.67 g (313 mmol) of triethylamine in 400 ml of methylene chloride. The temperature is not allowed to exceed 5° C. After addition is completed, it is stirred for 1 hour at 0° C., then for 2 hours at room temperature. 500 ml of ice water is added, and the water phase is set at pH 2 with 10% aqueous hydrochloric acid. The organic phase is separated, washed once each with 300 ml of 5% aqueous hydrochloric acid, 300 ml of 5% aqueous soda solution and 400 ml of water. The organic phase is dried on magnesium sulfate and evaporated to dryness in a vacuum. The residue recrystallizes from diisopropyl ether.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07211241B2uspto-grants-2007_05