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[ClH:1].OS(O)(=O)=O.[Na+].[Cl-].[CH3:9][C:10]([C:12]1[CH:13]=[CH:14][C:15]([OH:19])=[C:16]([OH:18])[CH:17]=1)=[O:11].O[C:21]1[CH:28]=[C:27]([OH:29])[CH:26]=[CH:25][C:22]=1[CH:23]=O>C(OCC)(=O)C>[Cl-:1].[OH:18][C:16]1[CH:17]=[C:12]([CH:13]=[CH:14][C:15]=1[OH:19])[C:10]1[CH:9]=[CH:23][C:22]2[C:25](=[CH:26][C:27]([OH:29])=[CH:28][CH:21]=2)[O+:11]=1참가 물질
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).
후처리
- customwas bubbled in a two-necked flask
- customto precipitate after 30 minutes
- waitThe solution was kept at −18° C. for 3 days
- filtrationit was filtered
- customThe filtrate was evaporated
- customthe product precipitated
- customIt was separated from the ether
- dissolutiondissolved in hot methanol
- additionit was added slowly to an equivalent volume of acetone
- customto precipitate
- filtrationAfter filtration
- customthe filtrate was evaporated
- dissolutiondissolved in a minimum of methanol
- additionether was added until a precipitate
출처 및 근거
- ORD 기록
- ord-cd034231b3244a81ab36790ecbdf8386
- 출처 데이터셋
- uspto-grants-2001_06
- 특허 번호
- US06241785B1
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