반응 #1064443

ord-1e4b4e8ed0cc47d69cd333423f2b7e99

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was refluxed under heating conditions for 4 hours
  2. 2
    농축After the reaction mixture was concentrated
  3. 3
    workup.ADDITIONchloroform was added to the residue
  4. 4
    세척the mixture was washed with 2 N HCl and water
  5. 5
    세척The chloroform layer was washed with water
  6. 6
    건조dried (MgSO4)
  7. 7
    농축concentrated

실험 절차

A mixture of 4-[2-(5-methyl-4-phenyl-2-thiazolyl)ethyl]cinnamaldehyde (2.5 g), 2,4-oxazolidinedione (1.14 g), piperidine (0.211 g) and ethanol (50 ml) was refluxed under heating conditions for 4 hours. After the reaction mixture was concentrated, chloroform was added to the residue; the mixture was washed with 2 N HCl and water. The chloroform layer was washed with water, dried (MgSO4) and then concentrated to yield 5-[4-[2-(5-methyl-4-phenyl-2-thiazolyl)ethyl]cinnamylidene]-2,4-oxazolidinedione[mixture of the (E)- and (Z)- configurations](0.81 g, 26%), which was then recrystallized from ethyl acetate to yield light yellow prisms having a melting point of 161°-162° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05614544uspto-grants-1997_03