Reaktion #81553

ord-47473cc55f5644b6b19ec0dd75be0af0

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled below 10° C.
  2. 2
    Sonstigekept below 12° C
  3. 3
    Sonstigereaction mixture
  4. 4
    ExtraktionProduct is extracted with ethyl acetate (2×50 mL), organic phases
  5. 5
    Einengenconcentrated in vacuo
  6. 6
    Sonstigethe residue chromatographed on silica gel (eluted with 10% ethyl acetate in hexane)

Vorschrift

To a solution of 4,4-dimethyl-7-hydroxy-1-tetralone (XIV) (3.07 g, 16.16 mmol) in water (10.77 mL) containing potassium hydroxide (904 mg) cooled below 10° C. was added N,N-dimethylthiocarbamoyl chloride (2.67 g, 21.6 mmol) in tetrahydrofuran (4.30 mL); the reaction temperature kept below 12° C. After 10 minutes, reaction mixture is made basic by the addition of a 10% aqueous KOH solution (5.39 mL). Product is extracted with ethyl acetate (2×50 mL), organic phases concentrated in vacuo and the residue chromatographed on silica gel (eluted with 10% ethyl acetate in hexane) to give 3.74 g (Y: 84%) of title product; 1H-NMR (CDCl3): δ7.68 (d, J=2.6 Hz, 1H), 7.45 (d, J=8.5 Hz, 1H), 7.27 (dd, J=8.5, 2.6 Hz, 1H), 3.46 (s, 3H), 3.34 (s, 3H), 2.73 (t, J=6.8 Hz, 2H), 2.04 (t, J=6.8 Hz, 2H), 1.41 (s, 6H); MS (DCI) m/e: 278 (MH+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05618839uspto-grants-1997_04