Dichloromethane → bis(4-oxo-2-phenyl-4H-chromen-3-yl)terephthalate

HRID 1925668

Reaktionsgleichung

Reaktionsgleichung von HRID 1925668
[OH:1][C:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[O:4][C:3]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[C:19](Cl)(=[O:29])[C:20]1[CH:28]=[CH:27][C:23]([C:24](Cl)=[O:25])=[CH:22][CH:21]=1.ClCCl.C(N([CH2:39][CH3:40])CC)C>O>[O:12]=[C:11]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[O:4][C:3]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)=[C:2]1[O:1][C:19](=[O:29])[C:20]1[CH:28]=[CH:27][C:23]([C:24]([O:1][C:2]2[C:11](=[O:12])[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[O:4][C:3]=2[C:40]2[CH:39]=[CH:18][CH:13]=[CH:14][CH:15]=2)=[O:25])=[CH:22][CH:21]=1

Komponenten

6

Versuchsvorschrift

To the three-necked round bottom flask attached with reflux condenser, calcium chloride guard tube and nitrogen inlet, 3-hydroxy-2-phenyl-4H-chromen-4-one (0.59 g), terephthaloyl chloride (0.59 g) and dichloromethane (50 ml) were charged. Then triethyl amine (0.29 g) was charged and the reaction mixture was stirred at room temperature and monitored by thin layer chromatography (TLC). On completion of the reaction 10 ml water was added to the reaction mixture and the organic layer was separated. The organic layer was dried and evaporated under reduced pressure to give the product.

Aufarbeitung

  1. temperaturewith reflux condenser, calcium chloride guard tube and nitrogen inlet
  2. additionwas added to the reaction mixture
  3. customthe organic layer was separated
  4. customThe organic layer was dried
  5. customevaporated under reduced pressure
  6. customto give the product

Quellen und Nachweise

ORD-Eintrag
ord-05698b17433241a3bb7f354098e0d834
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08178702B2

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