Benzaldehyde → 1-Hydroxy-3-phenylpropan-2-one

HRID 649731

Reaktionsgleichung

Reaktionsgleichung von HRID 649731
N[C@H](C=O)CCSC.C([O-])(=O)CC(CC([O-])=O)(C([O-])=O)O.[C:22]([O-:27])(=O)[C:23]([CH3:25])=[O:24].[Na+].C(=O)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>C(O)C>[C:30]1([CH2:25][C:23]([CH2:22][OH:27])=[O:24])[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

9.5 ml of 0.1 M citric acid and 40.5 ml of 0.1 M tri-sodium citrate were diluted to 100 ml to give a pH 6 citrate buffer solution. (Ref.: Buffers for pH and Metal Ion Control, D. D. Perrin and B. Dempsey, Publ. John Wiley and Sons, pg 103). Petroleum spirit (40 ml), ethanol (0.5 ml), the pH 6 citrate buffer (5 ml) and sodium pyruvate (2.5 g, 23 mmol) were stirred at room temperature for 1 h. Benzaldehyde (127 mg, 1.2 mmol) and baker's yeast (5 g) were then added and the reaction stirred at 5° C. for 24 h. The mixture was then filtered and yeast washed with diethyl ether. After removal of the solvent in vacuo the product was purified by flash distillation (200° C./1 mm) to give phenylacetylcarbinol (44 mg, 24%). The GC of the product showed pure PAC (11.88 min.). Chiral GC showed a ratio of 97.5:2.5, 95% ee.

Aufarbeitung

  1. filtrationThe mixture was then filtered
  2. washyeast washed with diethyl ether
  3. customAfter removal of the solvent in vacuo the product
  4. distillationwas purified by flash distillation (200° C./1 mm)

Quellen und Nachweise

ORD-Eintrag
ord-42be3edd5d01402192e1b9379fac1c4d
Quelldatensatz
uspto-grants-2001_08
Patentnummer
US06271008B1

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