StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Sodium Iodide → (S)-3-Hydroxy-4-iodobutanoic acid, methyl ester

HRID 327866
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 327866
Br[CH2:2][C@@H:3]([OH:9])[CH2:4][C:5]([O:7][CH3:8])=[O:6].[I-:10].[Na+]>C(C(C)=O)C>[OH:9][C@H:3]([CH2:2][I:10])[CH2:4][C:5]([O:7][CH3:8])=[O:6]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 5238Sodium IodideHCID 11960268methyl (S)-4-bromo-3-hydroxybutyrate

Produkt 1

HCID 86747447(S)-3-Hydroxy-4-iodobutanoic acid, methyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6569Methyl Ethyl KetoneLösungsmittel

Reaktionsbedingungen

Temperatur
92 °C

Versuchsvorschrift

A solution of (S)-4-Bromo-3-hydroxybutanoic acid, methyl ester (14.822 g, 75.2 mmol) in methyl ethyl ketone (255 mL) was treated with anhydrous sodium iodide (56.6 g, 376 mmol). The resulting red mixture was stirred for 23 hours under argon at a bath temperature of 92° C. The solution was allowed to cool to room temperature and the solids were filtered through celite. The receiver flask was switched and the celite bed was washed with ethyl acetate (3×50 mL). The original MEK product-rich filtrate was concentrated to approximately 60 mL. The residue was treated with the ethyl acetate wash from above followed by 250 mL of fresh ethyl acetate. The solution was washed with sodium sulfite solution (2×100 mL), brine (1×75 mL) and dried (sodium sulfate). Filtration followed by concentration in vacuo produced a yellow liquid which was evaporated several times from hexane and dried under high vacuum (5 mm) to 15.48 g (84%).

Aufarbeitung

  1. temperatureto cool to room temperature
  2. filtrationthe solids were filtered through celite
  3. washthe celite bed was washed with ethyl acetate (3×50 mL)
  4. concentrationThe original MEK product-rich filtrate was concentrated to approximately 60 mL
  5. additionThe residue was treated with the ethyl acetate
  6. washwash
  7. washThe solution was washed with sodium sulfite solution (2×100 mL), brine (1×75 mL)
  8. dry with materialdried (sodium sulfate)
  9. filtrationFiltration
  10. concentrationfollowed by concentration in vacuo
  11. customproduced a yellow liquid which
  12. customwas evaporated several times from hexane
  13. customdried under high vacuum (5 mm) to 15.48 g (84%)

Quellen und Nachweise

ORD-Eintrag
ord-672e1c42bc5349ceb79d42d09d2c4ca7
Quelldatensatz
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05274155

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion