反応 #1960489

ord-cabba34e4fc24024b91f0bcefd92dac5

反応方程式

CCCC1CCC(C2C=Cc3c4c(c(F)c(F)c3O2)OCCC4)CC1
5,6-difluoro-8-(4-propylcyclohexyl)-1,2,3,8-tetrahydropyrano[3,2-f]chromene
CCCC1CCC(C2CCc3c4c(c(F)c(F)c3O2)OCCC4)CC1
5,6-difluoro-3-(4-propylcyclohexyl)-1,2,3,8,9,10-hexahydropyrano[3,2-f]chromene

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The reaction solution is filtered
  2. 2
    その他the filtrate is evaporated to dryness
  3. 3
    その他The residue is purified by column chromatography (SiO2, n-heptane:1-chlorobutane=1:1)
  4. 4
    その他The further purification
  5. 5
    その他recrystallisation from n-heptane at 5° C.

実験手順

4.0 g (11.5 mmol) of 5,6-difluoro-8-(4-propylcyclohexyl)-1,2,3,8-tetrahydropyrano[3,2-f]chromene are hydrogenated at atmospheric pressure in THF and in the presence of Pd/C (5% of Pd). The reaction solution is filtered, and the filtrate is evaporated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:1-chlorobutane=1:1). The further purification is carried out by repeated recrystallisation from n-heptane at 5° C., giving 5,6-difluoro-3-(4-propylcyclohexyl)-1,2,3,8,9,10-hexahydropyrano[3,2-f]chromene as a colourless solid (m.p. 152° C.).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08303844B2uspto-grants-2012_11