反応 #93822

ord-431b0cdb38e74b3ca50046a77ca95cf3

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the mixture obtained
  2. 2
    温度is subsequently heated
  3. 3
    温度under reflux for about 30 minutes
  4. 4
    workup.WAITleft
  5. 5
    その他The porphine derivative is precipitated by the addition of 0.5 l of water
  6. 6
    その他The filtered-off crude product is pre-purified by two-fold column chromatography on 1.2 kg of silica gel, in each case
  7. 7
    洗浄the elution
  8. 8
    その他For the further purification
  9. 9
    ろ過filtered off
  10. 10
    その他The thus-obtained product is then chromatographed on a silica gel column

実験手順

15.2 ml of benzaldehyde and 7.51 g of 4-carboxybenzaldehyde are dissolved in 746 ml of boiling propionic acid, treated dropwise with 13.9 ml of pyrrole, the mixture obtained is subsequently heated under reflux for about 30 minutes and then left to cool to room temperature. The porphine derivative is precipitated by the addition of 0.5 l of water. The filtered-off crude product is pre-purified by two-fold column chromatography on 1.2 kg of silica gel, in each case the elution being carried out with the following solvents in sequence: chloroform/cyclohexane (1:1), chloroform/ethyl acetate (3:2) and (1:1), ethyl acetate and ethyl acetate which contains 2% methanol. For the further purification, the product is suspended in a small amount of methanol and filtered off. This procedure is repeated until the filtrate is only faintly coloured. The thus-obtained product is then chromatographed on a silica gel column using chloroform, chloroform/ethyl acetate (1:1) and ethyl acetate as the elution agent. There are obtained 1.7 g of 4-(10,15,20-triphenyl-21H,23H-porphin- 5-yl)benzoic acid as violet crystals.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04614723uspto-grants-1986_09