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Sodium Iodide → Iodomethyl Benzoate

HRID 2401193
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2401193
[C:1]([O:9][CH2:10]Cl)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[I-:12].[Na+]>C(#N)C.O>[C:1]([O:9][CH2:10][I:12])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 5238Sodium IodideHCID 79257Chloromethyl benzoate

Produkt 1

HCID 10015543Iodomethyl BenzoateAusbeute 71,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

Chloromethyl benzoate (2.87 g, 16.82 mmol) was dissolved in acetonitrile (20 mL) and treated portionwise with sodium iodide (5.04 g, 33.6 mmol). The resulting mixture was stirred at room temperature for 18 hours. The reaction mixture was diluted with water and extracted with ethyl acetate (×2). The ethyl acetate layers were combined, dried under magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography (Biotage SP4) eluting with a gradient of 0-20% ethyl acetate and iso-hexane. Product containing fractions were combined and evaporated under reduced pressure to give the title compound as a yellow oil (3.15 g);

Aufarbeitung

  1. extractionextracted with ethyl acetate (×2)
  2. customdried under magnesium sulfate
  3. customevaporated under reduced pressure
  4. customThe residue was purified by column chromatography (Biotage SP4)
  5. washeluting with a gradient of 0-20% ethyl acetate and iso-hexane
  6. additionProduct containing fractions
  7. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-08f072f24cdd4520a94b8a11359c627c
Quelldatensatz
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08796283B2

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