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Sodium Methoxide → (2S,3R)-3-(4-Benzyloxy-2-methyl-phenyl)-2-ethoxy-3-hydroxy-propionic acid methyl ester

HRID 1394665
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1394665
[CH3:1][O-:2].[Na+].C([C@H]1COC(=O)N1[C:17](=[O:39])[C@@H:18]([O:36][CH2:37][CH3:38])[C@@H:19]([C:21]1[CH:26]=[CH:25][C:24]([O:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)=[CH:23][C:22]=1[CH3:35])[OH:20])C1C=CC=CC=1>CO>[CH3:1][O:2][C:17](=[O:39])[C@@H:18]([O:36][CH2:37][CH3:38])[C@@H:19]([C:21]1[CH:26]=[CH:25][C:24]([O:27][CH2:28][C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)=[CH:23][C:22]=1[CH3:35])[OH:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 10942334Sodium MethoxideHCID 68616303(S)-4-Benzyl-3-[(2S,3R)-3-(4-benzyloxy-2-methyl-phenyl)-2-ethoxy-3-hydroxy-propionyl]-oxazolidin-2-one

Produkt 1

HCID 68616209(2S,3R)-3-(4-Benzyloxy-2-methyl-phenyl)-2-ethoxy-3-hydroxy-propionic acid methyl esterAusbeute 69,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A 5.4 M solution of sodium methoxide (7.3 ml, 39.5 mmol) was added to an ice-cooled and stirred suspension of (S)-4-benzyl-3-[(2S,3R)-3-(4-benzyloxy-2-methyl-phenyl)-2-ethoxy-3-hydroxy-propionyl]-oxazolidin-2-one (17.6 g, 36 mmol) in dry methanol (87 ml). The mixture was stirred at 0° C. for 15 min, quenched and neutralized by the addition of dilute aqueous hydrochloric acid (1.0 M). The solution was concentrated under reduced pressure and the residue dissolved in ice water/ethyl acetate 1/1. The layers were separated and the aqueous layer was extracted two times with ethyl acetate. The combined organic layers were washed with ice water and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, cyclohexane/AcOEt) to give 8.6 g (25 mmol, 69%) of the title compound as light yellow oil. According to 1H-NMR spectroscopy, one single diastereomer was obtained.

Aufarbeitung

  1. temperaturecooled
  2. stirringThe mixture was stirred at 0° C. for 15 min
  3. customquenched
  4. additionneutralized by the addition of dilute aqueous hydrochloric acid (1.0 M)
  5. concentrationThe solution was concentrated under reduced pressure
  6. dissolutionthe residue dissolved in ice water/ethyl acetate 1/1
  7. customThe layers were separated
  8. extractionthe aqueous layer was extracted two times with ethyl acetate
  9. washThe combined organic layers were washed with ice water
  10. dry with materialdried over sodium sulfate
  11. customThe solvent was removed under reduced pressure
  12. customthe residue purified by column chromatography (silica gel, cyclohexane/AcOEt)

Quellen und Nachweise

ORD-Eintrag
ord-5cd29e44331142519ad68c4b91fdc4c6
Quelldatensatz
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07348349B2

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