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Methanol → (R)-Methyl 2-(2-chlorophenyl)-2-hydroxyacetate

HRID 537386
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 537386
[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C@@H:4]([OH:8])[C:5]([OH:7])=[O:6].P(=O)(Cl)(Cl)Cl.[CH3:18]O>>[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C@@H:4]([OH:8])[C:5]([O:7][CH3:18])=[O:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 887MethanolHCID 24813Phosphorus oxychlorideHCID 2733641(-)-2-Chloromandelic acid

Produkt 1

HCID 11790232(R)-Methyl 2-(2-chlorophenyl)-2-hydroxyacetateAusbeute 95 %

Versuchsvorschrift

15 g of (R)-2-chloromandelic acid was mixed with methanol (CH3OH, 150 ml) and phosphorus chloride oxide (POCl3, 0.76 ml) in a flask by stirring using a magnetic stirrer at the room temperature for 6 hours. When the reaction was completed, the obtained product was washed with an aqueous solution of sodium sulfite (Na2SO3) and ethylacetate (EA). Then, the organic layer was dehydrated with anhydrous magnesium sulfate (MgSO4), filtrated, and concentrated under reduced pressure. The concentrated residue was purified by a silica gel column chromatography to produce the title compound (15.64 g, yield 95%).

Aufarbeitung

  1. customat the room temperature
  2. customfor 6 hours
  3. washthe obtained product was washed with an aqueous solution of sodium sulfite (Na2SO3) and ethylacetate (EA)
  4. filtrationfiltrated
  5. concentrationconcentrated under reduced pressure
  6. customThe concentrated residue was purified by a silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-25129f185ee64f75bede769f0a90c2d3
Quelldatensatz
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08859817B2

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