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Methanol → 5-(4-Fluoro-phenyl)-pentanoic acid methyl ester

HRID 2100506
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2100506
S(Cl)(Cl)=O.[F:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[CH:8][CH:7]=1.O.[CH3:20]O>>[CH3:20][O:17][C:16](=[O:18])[CH2:15][CH2:14][CH2:13][CH2:12][C:9]1[CH:8]=[CH:7][C:6]([F:5])=[CH:11][CH:10]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 887MethanolHCID 962WaterHCID 24386Thionyl ChlorideHCID 27346705-(4-Fluorophenyl)pentanoic acid

Produkt 1

HCID 685705095-(4-Fluoro-phenyl)-pentanoic acid methyl esterAusbeute 75 %

Versuchsvorschrift

Thionylchloride (288 μl, 3.98 mmol) was added dropwise to a solution of 5-(4-fluoro-phenyl)-pentanoic acid (520 mg, 2.65 mmol) in methanol (11 ml) at −15° C. The reaction mixture was then stirred at room temperature for 1.5 h. Water was added and the mixture was extracted 3 times with diethylether. The combined extracts were washed with water and brine, dried (Na2SO4) and evaporated. The remaining residue was purified by column chromatography (silica gel, ethyl acetate/heptane 5:95 to 12:88) to obtain 5-(4-fluoro-phenyl)-pentanoic acid methyl ester (420 mg, 2 mmol; 75%) as colorless liquid. MS: m/e 211.0 [M+H+].

Aufarbeitung

  1. extractionthe mixture was extracted 3 times with diethylether
  2. washThe combined extracts were washed with water and brine
  3. dry with materialdried (Na2SO4)
  4. customevaporated
  5. customThe remaining residue was purified by column chromatography (silica gel, ethyl acetate/heptane 5:95 to 12:88)

Quellen und Nachweise

ORD-Eintrag
ord-27480444f9d347468d44545597e2c8dc
Quelldatensatz
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07572801B2

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