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Ethyl 3,3,3-trifluoro-2-oxopropanoate → 2-Hydroxy-4-methyl-4-phenyl-2-trifluoromethylpentanoic acid ethyl ester

HRID 457273
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 457273
[CH3:1][C:2]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([CH3:6])[CH2:3][Mg]Cl.[F:13][C:14]([F:23])([F:22])[C:15](=[O:21])[C:16]([O:18][CH2:19][CH3:20])=[O:17]>C(OCC)C.C1COCC1>[CH2:19]([O:18][C:16](=[O:17])[C:15]([OH:21])([C:14]([F:13])([F:22])[F:23])[CH2:3][C:2]([CH3:1])([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[CH3:6])[CH3:20]
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Komponenten

5

Edukt 2

HCID 2737239Ethyl 3,3,3-trifluoro-2-oxopropanoateHCID 178418740HCID 178418740, Verbindung

Produkt 1

HCID 179356212-Hydroxy-4-methyl-4-phenyl-2-trifluoromethylpentanoic acid ethyl ester

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283Diethyl EtherLösungsmittel2×HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a room temperature solution of 45 mL (22.5 mmol) of a 0.5 M solution of 2-methyl-2-phenylpropylmagnesium chloride in diethyl ether was added 38 g (22.5 mmol) of ethyl trifluoropyruvate in 10 mL of anhydrous THF. The reaction became slightly warm to the touch and a white precipitate quickly developed. After 2 hours, the reaction was diluted with diethyl ether and quenched with 1 N aqueous HCl. The aqueous layer was separated and extracted with ether. The combined organic layers were dried over magnesium sulfate, filtered, and concentrated in vacuo to afford a brown oil. Chromatography on silica gel eluting with hexanes-EtOAc (98:2), afforded the title compound as a clear, colorless oil (4.6 g, 67%).

Aufarbeitung

  1. temperatureThe reaction became slightly warm to the touch
  2. customquenched with 1 N aqueous HCl
  3. customThe aqueous layer was separated
  4. extractionextracted with ether
  5. dry with materialThe combined organic layers were dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customto afford a brown oil

Quellen und Nachweise

ORD-Eintrag
ord-cad74846c480454c9ecca29daaad4d66
Quelldatensatz
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07186864B2

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