Boronic Acid → Ethyl 5,5,5-trifluoro-4-oxopentanoate

HRID 402904Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 402904
C(OC(=O)[CH:5]([C:12](=[O:17])[C:13]([F:16])([F:15])[F:14])[CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])C.B(O)O>C(O)C>[CH2:10]([O:9][C:7](=[O:8])[CH2:6][CH2:5][C:12](=[O:17])[C:13]([F:16])([F:15])[F:14])[CH3:11]

Komponenten

4

Reaktionsbedingungen

Temperatur
170 °C

Versuchsvorschrift

In a one-necked round-bottomed flask equipped with a distillation head and cooler, a mixture of 2-(2,2,2-trifluoro-acetyl)-succinic acid diethyl ester (54.6 g, 202 mmol) and boronic acid (12.5 g, 202 mmol) is heated to 170° C. Heating is continued for 4 h, during which time ethanol is gradually distilled off as it is formed. After cooling to room temperature, the reaction mixture is poured onto ice and extracted twice with EtOAc. The combined organic layers are washed with brine, dried over Na2SO4 and concentrated at reduced pressure to afford a brown oil. The crude product is purified by distillation (60° C., 10 mbar) to afford the title compound as a colorless liquid (17.3 g, 87.3 mmol, 43%). 1H NMR (400 MHz, CDCl3, 298 K): δ=4.15 (q, J=7.1 Hz, 2H), 3.02 (t, J=6.4 Hz, 2H), 2.70 (t, J=6.4 Hz, 2H), 1.45 (t, J=7.1 Hz, 3H). MS (ES+): 199 (M(C7H9F3O3)+H)+.

Aufarbeitung

  1. customIn a one-necked round-bottomed flask equipped with a distillation head and cooler
  2. temperatureHeating
  3. distillationis gradually distilled off as it
  4. customis formed
  5. temperatureAfter cooling to room temperature
  6. additionthe reaction mixture is poured onto ice
  7. extractionextracted twice with EtOAc
  8. washThe combined organic layers are washed with brine
  9. dry with materialdried over Na2SO4
  10. concentrationconcentrated at reduced pressure
  11. customto afford a brown oil
  12. distillationThe crude product is purified by distillation (60° C., 10 mbar)

Quellen und Nachweise

ORD-Eintrag
ord-715a9f1dc86d4bf6b8c027be82a75155
Quelldatensatz
uspto-grants-2014_06
Patentnummer
US08742132B2

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