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Chloride → 4-Carbomethoxymethyl azetidin-2-one

HRID 648685
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 648685
[Cl-].[Si]([N:9]1[C@H:12]([CH2:13][C:14](SC)(SC)SC)[C@@H:11]([C@H](O)C)[C:10]1=[O:24])(C(C)(C)C)(C)C.[C:25](=O)(O)[O-:26].[Na+].C[OH:31]>>[C:14]([CH2:13][CH:12]1[NH:9][C:10](=[O:24])[CH2:11]1)([O:26][CH3:25])=[O:31]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 312ChlorideHCID 887MethanolHCID 516892Sodium BicarbonateHCID 13104625(3S,4R)-1-(t-butyldimethylsilyl)3-[(R)-1-hydroxyethyl]-4-[2,2,2-tri(methylthio)ethyl]azetidin-2-one

Produkt 1

HCID 128327374-Carbomethoxymethyl azetidin-2-one

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Mecuric chloride (12.37 g, 45.6 mmol) is added in one portion to a solution of (3S, 4R)-1-(t-butyldimethylsilyl)-3-[(R)-1-hydroxyethyl]-4-[2,2,2-tri(methylthio)ethyl]azetidin-2-one (6.0 g, 15.2 mmol) in 250 ml of absolute methanol at 0° C. The resulting mixture (heavy white precipitate) is stirred at 0° C. for 3 min., then quenched by addition of sodium bicarbonate (8.99 g, 107 mmol). This mixture is then filtered and the solid residue is washed with additional methanol. The combined filtrate and washings are concentrated in vacuo and the residue is partitioned between ethyl acetate and saturated aqueous ammonium chloride solution. The organic phase is separated, washed with saturated aqueous ammonium chloride solution, water and brine and dried over magnesium sulfate. Removal of solvents in vacuo gives an oil which is chromatographed on a silica gel column (3:2 cyclohexane:ethyl acetate) to yield (3S, 4R)-1-(t-butyldimethylsilyl)-3-[(R)-1-hydroxyethyl)]-4-carbomethoxymethyl azetidin-2-one.

Aufarbeitung

  1. filtrationThis mixture is then filtered
  2. washthe solid residue is washed with additional methanol
  3. concentrationThe combined filtrate and washings are concentrated in vacuo
  4. customthe residue is partitioned between ethyl acetate and saturated aqueous ammonium chloride solution
  5. customThe organic phase is separated
  6. washwashed with saturated aqueous ammonium chloride solution, water and brine
  7. dry with materialdried over magnesium sulfate
  8. customRemoval of solvents in vacuo
  9. customgives an oil which
  10. customis chromatographed on a silica gel column (3:2 cyclohexane:ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-146ac05791104201a1aeb6525a3f2b7a
Quelldatensatz
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04736025

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