反应 #1884944

ord-bf937a21c427441e9d6260f0201adc71

反应方程式

C=CCSCCNC(=O)CCn1cccc1
N-(2-Allylsulfanyl-ethyl)-3-pyrrol-1-yl-propionamide
O=C(OO)c1cccc(Cl)c1
Meta-chloroperoxybenzoic acid
O=C(O)c1cccc(Cl)c1
meta-chlorobenzoic acid
收率 60.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction mixture was cooled to between 0-4 C
  2. 2
    workup.STIRRINGthe reaction stirred at 0-4 C for 16 hours
  3. 3
    其他The solvent was removed in vacuo and purification by flash chromatography on silica
  4. 4
    洗涤eluting with ethyl acetate

实验过程

N-(2-Allylsulfanyl-ethyl)-3-pyrrol-1-yl-propionamide (0.3704 g, 1.554 mmol, 1 equiv) was taken up in 100 ml of dichloromethane with stirring under nitrogen. The reaction mixture was cooled to between 0-4 C. Meta-chloroperoxybenzoic acid (0.4815 g, 2.790 mmol, 1.8 equiv) was added to the mixture and the reaction stirred at 0-4 C for 16 hours. The solvent was removed in vacuo and purification by flash chromatography on silica: eluting with ethyl acetate gave the by-product meta-chlorobenzoic acid. Further elution with the solvent mixture was gradually changed to a 1:1 ethyl acetate/ethanol gave the product which was isolated by removal of the solvent in vacuo as off-white crystals in 60% yield.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08343212B2uspto-grants-2013_01