Reaction #2139951

ord-fb0d8d027bae4846bae619fed066a54b

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    FiltrationThe solution was subsequently filtered through silica gel
  2. 2
    Otherevaporated
  3. 3
    Otherthe crude product was purified by crystallisation from MTB ether

Procedure

11.7 g (25.6 mmol) of 3-butoxy-4,7-difluoro-8-(4-pentylcyclohexyl)-benzo[c]chromen-6-one and 11.4 g (28.2 mmol) of Lawesson's reagent were refluxed for 16 hours in 130 ml of chlorobenzene. The solution was subsequently filtered through silica gel and evaporated, and the crude product was purified by crystallisation from MTB ether, giving 7.9 g (65%) of 3-butoxy-4,7-difluoro-8-(4-pentylcyclohexyl)benzo[c]chromene-6-thione as yellow crystals.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07326447B2uspto-grants-2008_02