Pyruvic Acid → 2,2-Diethoxypropionic acid

HRID 30521

Reaktionsgleichung

Reaktionsgleichung von HRID 30521
[C:1]([OH:6])(=[O:5])C(C)=O.C(O[CH:10]([O:14][CH2:15][CH3:16])[O:11][CH2:12][CH3:13])C.S(=O)(=O)(O)O.Cl[CH2:23]Cl>>[CH2:15]([O:14][C:10]([O:11][CH2:12][CH3:13])([CH3:23])[C:1]([OH:6])=[O:5])[CH3:16]

Komponenten

5

Reaktionsbedingungen

Temperatur
7.5 °C

Versuchsvorschrift

To a stirred solution of pyruvic acid (14 mL, 0.2 mol) and triethylorthoformate (80 mL) at 10° C. was added concentrated sulfuric acid (1 mL). The resulting mixture was stirred at 5-10° C. for 1 h and then diluted with dichloromethane (200 mL). The organic solution was washed successively with water (3×80 mL) and saturated sodium chloride solution (80 mL) and then dried over anhydrous sodium sulfate. The mixture was filtered and then concentrated to give a quantitative yield of 2,2-diethoxypropionic acid as an oil. 1H NMR (CDCl3, 400 MHz): δ 1.30 (t, 6H), 1.61 (s, 3H), 3.57 (q, 4H), 8.62 (s, 1H). The acid form was quantitatively converted to its cesium salt (25) by dissolving the acid in water (25 mL) followed by treatment with an equimolar quantity of cesium carbonate, and then lyophilization. 1H NMR (D2O, 400 MHz): δ 0.98 (t, 6H), 1.28 (s, 3H), 3.22 (q, 2H), 3.47 (q, 2H).

Aufarbeitung

  1. washThe organic solution was washed successively with water (3×80 mL) and saturated sodium chloride solution (80 mL)
  2. dry with materialdried over anhydrous sodium sulfate
  3. filtrationThe mixture was filtered
  4. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-2e0068e926734109bd32641036c37977
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07423169B2

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