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Sodium Iodide → (4S,5S)-4-[(Benzyloxy)methyl]-5-(iodomethyl)-2,2-dimethyl-1,3-dioxolane

HRID 1695019
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1695019
CS(O[CH2:6][C@H:7]1[C@H:11]([CH2:12][O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[O:10][C:9]([CH3:22])([CH3:21])[O:8]1)(=O)=O.[I-:23].[Na+]>C(#N)C>[CH2:14]([O:13][CH2:12][C@H:11]1[C@@H:7]([CH2:6][I:23])[O:8][C:9]([CH3:22])([CH3:21])[O:10]1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 5238Sodium IodideHCID 14731143{(4S,5S)-5-[(Benzyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl methanesulfonate2×

Produkt 1

HCID 66645664(4S,5S)-4-[(Benzyloxy)methyl]-5-(iodomethyl)-2,2-dimethyl-1,3-dioxolaneAusbeute 97,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A solution of 46.19 g of the crude {(4S,5S)-5-[(benzyloxy)methyl]-2,2-dimethyl-1,3-dioxolan-4-yl}methyl methanesulfonate obtained in Reference Example (1b) (140 mmol) and 62.87 g of sodium iodide (419 mmol) in acetonitrile (420 ml) was stirred at 80° C. for 22 hours. The reaction mixture was cooled and then concentrated under reduced pressure and diluted with water, followed by extraction with ethyl acetate. Then, the organic layer was washed with a 1.5 M sodium sulfite aqueous solution, water and brine and dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure to obtain 49.20 g of the crude title compound.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled
  2. concentrationconcentrated under reduced pressure
  3. additiondiluted with water
  4. extractionfollowed by extraction with ethyl acetate
  5. washThen, the organic layer was washed with a 1.5 M sodium sulfite aqueous solution, water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationAfter filtration
  8. customthe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-719b9f5962c04e8f9d619a99a23a8704
Quelldatensatz
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08158790B2

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