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

HRID 916003
Notes
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Reaction equation

HRID 916003 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolvent2×HCID 8028TetrahydrofuranSolvent

Procedure

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%).

Workup

  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

Sources & evidence

ORD record
ord-08c23dde441642368a02464d4a262e5f
Source dataset
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07268152B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes