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Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 71246625, Verbindung

HRID 1620764
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1620764
[OH:1][C:2]1([C@H:5]2[CH2:9][O:8]C(C)(C)[N:6]2[C:12]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[O:13])[CH2:4][CH2:3]1.CC1C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.C(=O)([O-])O.[Na+]>CO>[CH2:15]([O:14][C:12](=[O:13])[NH:6][C@@H:5]([C:2]1([OH:1])[CH2:3][CH2:4]1)[CH2:9][OH:8])[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
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Komponenten

5

Edukt 3

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 516892Sodium BicarbonateHCID 11460510HCID 11460510, Verbindung

Produkt 1

HCID 71246625HCID 71246625, VerbindungAusbeute 79,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of benzyl(4R)-4-(1-hydroxycyclopropyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (2.45 g) in methanol (100 mL) was added pyridin-1-ium 4-methylbenzenesulfonate (2.33 g) at room temperature. The reaction mixture was stirred at room temperature overnight, to the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was separated, washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.68 g).

Aufarbeitung

  1. extractionthe mixture was extracted with ethyl acetate
  2. customThe organic layer was separated
  3. washwashed with saturated brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-085e1b5cc91a43919c98b6befa203090
Quelldatensatz
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08772277B2

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