Reaktion #4496

ord-d744f03ba5db41d1bd7902f811b93a8d

Reaktionsgleichung

NC(=S)C1CCCCC1
cyclohexanethiocarboxamide
CCOC(=O)CC(=O)CCl
ethyl 4-chloroacetoacetate
CCOC(=O)Cc1csc(C2CCCCC2)n1
ethyl 2-cyclohexyl-4-thiazoleacetate
Ausbeute 71.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturunder reflux for 1 hour
  3. 3
    ExtraktionAfter dilution with water, mixture was extracted with ethyl acetate
  4. 4
    WaschenThe extract was washed with aqueous sodium bicarbonate solution and water
  5. 5
    Trocknendried (MgSO4)
  6. 6
    Einengenconcentrated
  7. 7
    SonstigeThe residue was purified by chromatography on silica gel with ethyl acetate-hexane (1:4)

Vorschrift

A mixture of cyclohexanethiocarboxamide (5.0 g), ethyl 4-chloroacetoacetate (5.74 g), ethanol (50 ml) was heated under reflux for 1 hour. After dilution with water, mixture was extracted with ethyl acetate. The extract was washed with aqueous sodium bicarbonate solution and water, dried (MgSO4), and concentrated. The residue was purified by chromatography on silica gel with ethyl acetate-hexane (1:4) to yield ethyl 2-cyclohexyl-4-thiazoleacetate as an oil (6.3 g, 70.9%). IR (Neat): 1735, 1255 cm-1. NMR (CDCl3)δ: 1.28 (3H, t, J=7 Hz), 1.2-2.3 (10H, m), 2.97 (1H, m), 3.77 (2H, s), 4.17 (2H, q, J=7 Hz), 7.0 (1H, s).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04725610uspto-grants-1988_02