تفاعل #2139951

ord-fb0d8d027bae4846bae619fed066a54b

معادلة التفاعل

CCCCCC1CCC(c2ccc3c(c2F)c(=O)oc2c(F)c(OCCCC)ccc23)CC1
3-butoxy-4,7-difluoro-8-(4-pentylcyclohexyl)-benzo[c]chromen-6-one
COc1ccc(P2(=S)SP(=S)(c3ccc(OC)cc3)S2)cc1
Lawesson's reagent
CCCCCC1CCC(c2ccc3c(c2F)c(=S)oc2c(F)c(OCCCC)ccc23)CC1
3-butoxy-4,7-difluoro-8-(4-pentylcyclohexyl)benzo[c]chromene-6-thione
المردود 65.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe solution was subsequently filtered through silica gel
  2. 2
    أخرىevaporated
  3. 3
    أخرىthe crude product was purified by crystallisation from MTB ether

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07326447B2uspto-grants-2008_02