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Dimethylformamide → Methyl 2-methyl-3-(methylthio)-4-(pentafluoroethyl)benzoate

HRID 1910383
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1910383
F[C:2]1[C:3]([CH3:19])=[C:4]([CH:9]=[CH:10][C:11]=1[C:12]([F:18])([F:17])[C:13]([F:16])([F:15])[F:14])[C:5]([O:7][CH3:8])=[O:6].CN(C=O)C.[CH3:25][S-:26].[Na+]>C(OCC)(=O)C>[CH3:19][C:3]1[C:2]([S:26][CH3:25])=[C:11]([C:12]([F:18])([F:17])[C:13]([F:16])([F:15])[F:14])[CH:10]=[CH:9][C:4]=1[C:5]([O:7][CH3:8])=[O:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 4378561Sodium methanethiolateHCID 86661429HCID 86661429, Verbindung

Produkt 1

HCID 86661431Methyl 2-methyl-3-(methylthio)-4-(pentafluoroethyl)benzoateAusbeute 55,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

2.1 g (7.34 mmol) of methyl 3-fluoro-2-methyl-4-(pentafluoroethyl)benzoate were introduced into 20 ml of DMF and then admixed with 758 mg (95% by weight; 10.3 mmol) of sodium thiomethoxide. The mixture was stirred at RT for 2 hours and then freed from the solvent. The residue was taken up in ethyl acetate and water, the aqueous phase was extracted twice with ethyl acetate, and, finally, the combined organic phases were dried and freed from the solvent. The residue was purified by chromatography, giving 1.28 g of clean product.

Aufarbeitung

  1. extractionwater, the aqueous phase was extracted twice with ethyl acetate
  2. customfinally, the combined organic phases were dried
  3. customThe residue was purified by chromatography

Quellen und Nachweise

ORD-Eintrag
ord-58bdfdde49ed482493d985ad0a0b98b7
Quelldatensatz
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08603947B2

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