Reaktion #1844398

ord-1ddff3fd1a5b4a6684a52f905c20f779

Reaktionsgleichung

Cl
HCl
CSc1ccc(CBr)cc1
4-methylthiobenzyl bromide
O=C1CSC(=O)C1
thiotetronic acid
[K+].[OH-]
potassium hydroxide
CSc1ccc(CC2=C(O)CSC2=O)cc1
solid
Ausbeute 26.5%
CSc1ccc(CC2=C(O)CSC2=O)cc1
4-Hydroxy-3-[[4-(methylthio)phenyl]methyl]-2(5H)-thiophenone
Ausbeute 26.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with EtOAc
  2. 2
    TrocknenThe organic extracts were dried over MgSO4
  3. 3
    SonstigeEvaporation and purification by flash chromatography on acid
  4. 4
    Waschenwashed (5% H3PO4 in MeOH) silica gel (eluting solvent hexane/EtOAc 1/3)

Vorschrift

To a suspension of 4-methylthiobenzyl bromide (5.6 g. 25.8 mmol), thiotetronic acid (3.0 g, 25.8 mmol) in dioxane (50 ml), was added aqueous potassium hydroxide (25.8 mL). The mixture was stirred at temperatures in the range of 65°-70° C. for 3 hours. Then, the mixture was cooled to room temperature, poured into H2O, acidified with HCl (2N) and extracted with EtOAc. The organic extracts were dried over MgSO4. Evaporation and purification by flash chromatography on acid washed (5% H3PO4 in MeOH) silica gel (eluting solvent hexane/EtOAc 1/3) gave a white solid (1.72 g, 26.5%): m.p. 206°-208° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05444086uspto-grants-1995_08