반응 #1153144

ord-cd034231b3244a81ab36790ecbdf8386

반응 방정식

Cl
hydrochloric acid
O=S(=O)(O)O
H2SO4
[Cl-].[Na+]
NaCl
CC(=O)c1ccc(O)c(O)c1
3,4-dihydroxyacetophenone
O=Cc1ccc(O)cc1O
2,4-dihydroxybenzaldehyde
Oc1ccc2ccc(-c3ccc(O)c(O)c3)[o+]c2c1.[Cl-]
3′,4′,7-trihydroxyflavylium chloride
수율 75.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타was bubbled in a two-necked flask
  2. 2
    기타to precipitate after 30 minutes
  3. 3
    workup.WAITThe solution was kept at −18° C. for 3 days
  4. 4
    여과it was filtered
  5. 5
    기타The filtrate was evaporated
  6. 6
    기타the product precipitated
  7. 7
    기타It was separated from the ether
  8. 8
    workup.DISSOLUTIONdissolved in hot methanol
  9. 9
    workup.ADDITIONit was added slowly to an equivalent volume of acetone
  10. 10
    기타to precipitate
  11. 11
    여과After filtration
  12. 12
    기타the filtrate was evaporated
  13. 13
    workup.DISSOLUTIONdissolved in a minimum of methanol
  14. 14
    workup.ADDITIONether was added until a precipitate

실험 절차

At 0° C., hydrochloric acid (generated by dropwise addition of H2SO4 to NaCl) was bubbled in a two-necked flask containing 12 g (0.079 mol) of 3,4-dihydroxyacetophenone, 10.88 g (0.079 mol) of 2,4-dihydroxybenzaldehyde and 100 ml of ethyl acetate distilled beforehand. The product started to precipitate after 30 minutes. The bubbling was continued for another 1 hour and then the reaction was stopped. The solution was kept at −18° C. for 3 days and then it was filtered. The filtrate was evaporated and it was taken up in ether; the product precipitated. It was separated from the ether, dissolved in hot methanol and then it was added slowly to an equivalent volume of acetone. The solution was placed in a refrigerator and the product started to precipitate. After filtration, the filtrate was evaporated, dissolved in a minimum of methanol and then ether was added until a precipitate appeared. The procedure was thus repeated several times until precipitate no longer appeared. The purity of the 3′,4′,7-trihydroxyflavylium chloride precipitate thus obtained with a yield of 75% was checked by HPLC (high-performance liquid chromatography).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06241785B1uspto-grants-2001_06