Sulfuric Acid → 3-benzyl-6,7-dihydroxy-4-methyl-2H-chromen-2-one

HRID 1595135

Reaktionsgleichung

Reaktionsgleichung von HRID 1595135
C([O:4][C:5]1[CH:10]=CC(OC(=O)C)=[CH:7][C:6]=1[O:15]C(=O)C)(=O)C.[CH2:19]([CH:26]([C:32]([CH3:34])=O)[C:27]([O:29][CH2:30][CH3:31])=[O:28])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.S(=O)(=O)(O)O>>[OH:4][C:5]1[CH:10]=[C:31]2[C:30](=[CH:7][C:6]=1[OH:15])[O:29][C:27](=[O:28])[C:26]([CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[C:32]2[CH3:34]

Komponenten

4

Edukt 3

HCID 1118Sulfuric AcidHCID 691691,2,4-TriacetoxybenzeneHCID 246929Ethyl alpha-benzylacetoacetate

Produkt 1

HCID 163946973-benzyl-6,7-dihydroxy-4-methyl-2H-chromen-2-one

Versuchsvorschrift

1,2,4-triacetoxybenzene (6.3 g, 25 mmol) and ethyl 2-benzylacetoacetate (5.5 g, 25 mmol) were heated together as described in Example 1. 75% sulphuric acid (35 ml) was added to the stirred solution and stirring continued for 16 hours. The dark coloured suspension was poured into ice/water (350 ml) with good stirring and the grey suspension filtered and the residue washed with abundant water. The residual solid was air dried and recrystallised from hot ethanol with subsequent addition of a little water to aid crystallization. The esculetin derivative formed small white needles (5.5 g, 75.3%).

Aufarbeitung

  1. stirringwith good stirring
  2. filtrationthe grey suspension filtered
  3. washthe residue washed with abundant water
  4. customdried
  5. customrecrystallised from hot ethanol with subsequent addition of a little water
  6. customcrystallization

Quellen und Nachweise

ORD-Eintrag
ord-9fd58c97fca9431ba35debecc4e8df3d
Quelldatensatz
uspto-grants-2001_09
Patentnummer
US06287798B1

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