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Sodium Iodide → 1-[2-(3-Methyl-2-nitrophenoxy)-ethyl]-pyrrolidine

HRID 6949
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 6949
C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].[CH3:9][C:10]1[C:11]([N+:17]([O-:19])=[O:18])=[C:12]([OH:16])[CH:13]=[CH:14][CH:15]=1.Cl.Cl[CH2:22][CH2:23][N:24]1[CH2:28][CH2:27][CH2:26][CH2:25]1>>[CH3:9][C:10]1[C:11]([N+:17]([O-:19])=[O:18])=[C:12]([CH:13]=[CH:14][CH:15]=1)[O:16][CH2:22][CH2:23][N:24]1[CH2:28][CH2:27][CH2:26][CH2:25]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 5238Sodium IodideHCID 11430Potassium Carbonate2×HCID 210263-Methyl-2-nitrophenolHCID 816681-(2-Chloroethyl)pyrrolidine hydrochloride2×

Produkt 1

HCID 116012601-[2-(3-Methyl-2-nitrophenoxy)-ethyl]-pyrrolidineAusbeute 69 %

Versuchsvorschrift

Potassium carbonate (34.9 g., 252 mmol) and sodium iodide (1.0 g., 6.5 mmol) were added to a solution of 3-methyl-2-nitrophenol (10 g., 65.3 mmol). With stirring, 1-(2-chloroethyl)-pyrrolidine hydrochloride (16.65 g., 98 mmol) was added portion-wise to the solution. The reaction mixture was refluxed for 15 hours, at which time 1-(2-chloroethyl)-pyrrolidine hydrochloride (8.5 g., 50 mmol) and potassium carbonate (18 g., 130 mmol) were added. After an additional hour of reflux, the reaction mixture was allowed to cool to room temperature and was washed with sequentially with water (1×100 mL) and brine (1×100 mL.) The combined organic fractions spontaneously crystallized, and the solid was purified by flash chromatography (5% MeOH in CH2Cl2) to give 1-[2-(3-Methyl-2-nitrophenoxy)-ethyl]-pyrrolidine (10.291 g., 69%). MS: 251 (M+H)+

Aufarbeitung

  1. additionwere added
  2. temperatureAfter an additional hour of reflux
  3. washwas washed with sequentially with water (1×100 mL) and brine (1×100 mL.) The combined organic fractions
  4. customspontaneously crystallized
  5. customthe solid was purified by flash chromatography (5% MeOH in CH2Cl2)

Quellen und Nachweise

ORD-Eintrag
ord-053aef3bb4e14e958a06b1ca6a830675
Quelldatensatz
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07084169B2

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