反应 #2200609

ord-e70bd3b180264aec8401e55b8b615636

反应方程式

[Na+].[OH-]
Sodium hydroxide
C1CCNC1
Pyrrolidine
O=C(Cl)CCl
chloroacetyl chloride
O=C(Cl)CCl
chloroacetyl chloride
O=C(CCl)N1CCCC1
N-(chloroacetyl)pyrrolidine
收率 48.6%

溶剂

反应条件

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

后处理

  1. 1
    温度dropwise maintaining the internal temperature below 15° C
  2. 2
    workup.STIRRINGwith vigorous stirring such that the inside temperature
  3. 3
    其他did not exceed 20° C
  4. 4
    workup.STIRRINGThe mixture was stirred for 15 minutes
  5. 5
    其他the aqueous layer was separated
  6. 6
    洗涤The organic layer was washed with saturated sodium bicarbonate solution (2×200 mL), water (1×200 mL)
  7. 7
    干燥dried over anhydrous sodium sulfate
  8. 8
    其他The solvent was removed in vacuo
  9. 9
    其他the residue was recrystallized from hexane
  10. 10
    其他to give 64.5 g (48.6% yield) of white plate crystals

实验过程

Pyrrolidine (63.9 g, 0.9 mole) was taken up in CH2Cl2 (640 mL) and cooled to 0° C. in a salt-ice water bath. To the stirred mixture was added chloroacetyl chloride (101.8 g in 450 mL of CH2Cl2, 0.9 mole) dropwise maintaining the internal temperature below 15° C. After adding the chloroacetyl chloride, the mixture was stirred for one hour at 5° C. Sodium hydroxide solution (7 M, 190 mL) was added with vigorous stirring such that the inside temperature did not exceed 20° C. The mixture was stirred for 15 minutes and the aqueous layer was separated. The organic layer was washed with saturated sodium bicarbonate solution (2×200 mL), water (1×200 mL) and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was recrystallized from hexane to give 64.5 g (48.6% yield) of white plate crystals; mp 43° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07432254B2uspto-grants-2008_10