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Dimethylformamide → N,N-dimethyl-N-{2-[(4-nitrophenyl)thio]ethyl}amine

HRID 2236688
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2236688
Cl.CN([CH:5]([SH:7])C)C.C(=O)([O-])[O-].[K+].[K+].F[C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=1.[CH3:24][N:25]([CH3:28])[CH:26]=O>O>[CH3:24][N:25]([CH3:28])[CH2:26][CH2:5][S:7][C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 9590p-FluoronitrobenzeneHCID 11430Potassium CarbonateHCID 22036395N,N-dimethylaminoethanethiol hydrochloride

Produkt 1

HCID 21204381N,N-dimethyl-N-{2-[(4-nitrophenyl)thio]ethyl}amineAusbeute 72 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel

Versuchsvorschrift

To a solution of N,N-dimethylaminoethanethiol hydrochloride (2.9 g, 14 mmol) in N,N-dimethylformamide (DMF) (70 mL) is added potassium carbonate (19 g, 140 mmol), followed by 4-fluoronitrobenzene (1.5 mL, 14 mmol). After stirring overnight at room temperature, the reaction mixture is diluted with water and extracted 3× with ethyl acetate. The combined extracts were washed five times with water and with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The crude oil is purified by flash chromatography (Isco 40 g Redi-Sep column, MeOH/CHCl3) to give N,N-dimethyl-N-{2-[(4-nitrophenyl)thio]ethyl}amine (2.3 g, 72%) as a golden oil.

Aufarbeitung

  1. extractionextracted 3× with ethyl acetate
  2. washThe combined extracts were washed five times with water
  3. dry with materialwith saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe crude oil is purified by flash chromatography (Isco 40 g Redi-Sep column, MeOH/CHCl3)

Quellen und Nachweise

ORD-Eintrag
ord-ddda25bdc3124b2ba48f4f0b3b6cda05
Quelldatensatz
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07713994B2

Notizen zur Reaktion

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