Tributylamine → Resveratrol

HRID 1949331

Reaktionsgleichung

Reaktionsgleichung von HRID 1949331
[Cl-].[Al+3].[Cl-].[Cl-].C(N(CCCC)CCCC)CCC.C[O:19][C:20]1[CH:21]=[C:22](/[CH:28]=[CH:29]/[C:30]2[CH:35]=[CH:34][C:33]([O:36]C)=[CH:32][CH:31]=2)[CH:23]=[C:24]([O:26]C)[CH:25]=1>>[C:22]1(/[CH:28]=[CH:29]/[C:30]2[CH:35]=[CH:34][C:33]([OH:36])=[CH:32][CH:31]=2)[CH:23]=[C:24]([OH:26])[CH:25]=[C:20]([OH:19])[CH:21]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
2.5 °C

Versuchsvorschrift

4.5 g of anhydrous aluminium chloride (33.7 mmol) are introduced, under a nitrogen atmosphere, at ambient temperature and with stirring, into 10.37 g of tributylamine (56 mmol) in a three-necked round-bottomed flask. The medium is brought to 60° C. and is maintained at this value for 4 h. 1 g of (E)-3,5,4′-trimethoxystilbene (3.7 mmol) is then introduced and the reaction medium is brought to 80° C. for 2 h and to 100° C. for 2 h. It is brought back to ambient temperature and then 10 g of a 50/50 water/ice mixture are added. It is maintained at 0-5° C. with stirring for 3 h and extracted 4 to 5 times with 10 ml of methyl ethyl ketone. The combined organic phases are washed with 10 ml of a saturated aqueous sodium bicarbonate solution and then with 10 ml of water. After concentrating the organic phase, an HPLC quantitative determination (external calibration) gives an (E)-resveratrol yield of 75%.

Aufarbeitung

  1. customis brought to 60° C.
  2. temperatureis maintained at this value for 4 h
  3. customis brought back to ambient temperature
  4. extractionextracted 4 to 5 times with 10 ml of methyl ethyl ketone
  5. washThe combined organic phases are washed with 10 ml of a saturated aqueous sodium bicarbonate solution
  6. concentrationAfter concentrating the organic phase

Quellen und Nachweise

ORD-Eintrag
ord-e383b14e825a47729212ae0eb6abd845
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08399714B2

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