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Sulfuric Acid → (R)-2-Hydroxy-3-(4-methoxy-phenyl)-propionic acid ethyl ester

HRID 1942473
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1942473
[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]([CH2:7][C@H:8]([C:10]([OH:12])=[O:11])N)=[CH:5][CH:4]=1.S(=O)(=O)(O)O.N([O-])=O.[Na+].C(=O)([O-])[OH:25].[Na+].O1CCO[CH2:31][CH2:30]1>>[OH:25][C@H:8]([CH2:7][C:6]1[CH:13]=[CH:14][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)[C:10]([O:12][CH2:30][CH3:31])=[O:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 1118Sulfuric AcidHCID 312751,4-DioxaneHCID 516892Sodium BicarbonateHCID 6950205O-Methyl-D-tyrosineHCID 23668193Sodium Nitrite

Produkt 1

HCID 29949072(R)-2-Hydroxy-3-(4-methoxy-phenyl)-propionic acid ethyl ester

Versuchsvorschrift

Commercially available O-methyl-D-tyrosine (5.00 g) was dissolved in 1,4-dioxane (62.5 ml), and thereto were added successively dropwise an aqueous sulfuric acid solution (5.4 g/17.5 ml of water) and an aqueous sodium nitrite solution (6.3 g/15.0 ml of water) under ice-cooling, and the mixture was stirred at room temperature. Ten hours later, to the reaction solution was added a saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over sodium hydrogen sulfate, filtered, and concentrated under reduced pressure. The resultant was duly dried, and then, the obtained residue was dissolved in ethanol (50 ml), and further thereto was added conc. sulfuric acid (200 μL). The mixture was refluxed for 15 hours, and the reaction solution was added dropwise into ice-water (50 ml), and the mixture was extracted with ethyl acetate (50 ml). The organic layer was washed successively with a saturated aqueous sodium hydrogen carbonate solution and a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (the developing solvent: hexane/ethyl acetate=5/1) to give the title compound (3.40 g) as a colorless liquid.

Aufarbeitung

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with a saturated aqueous sodium chloride solution
  3. dry with materialdried over sodium hydrogen sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe resultant was duly dried
  7. dissolutionthe obtained residue was dissolved in ethanol (50 ml)
  8. additionfurther thereto was added conc. sulfuric acid (200 μL)
  9. temperatureThe mixture was refluxed for 15 hours
  10. additionthe reaction solution was added dropwise into ice-water (50 ml)
  11. extractionthe mixture was extracted with ethyl acetate (50 ml)
  12. washThe organic layer was washed successively with a saturated aqueous sodium hydrogen carbonate solution
  13. dry with materiala saturated aqueous sodium chloride solution, dried over sodium sulfate
  14. filtrationfiltered
  15. concentrationconcentrated under reduced pressure
  16. customThe obtained residue was purified by silica gel column chromatography (the developing solvent

Quellen und Nachweise

ORD-Eintrag
ord-f95f0cd06f084ed694df7e543025003c
Quelldatensatz
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08389511B2

Notizen zur Reaktion

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