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Sodium methanethiolate → 2-[[2-(Methylthio)-3-pyridinyl]oxy]ethanol

HRID 1789758
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Reaktionsgleichung

Reaktionsgleichung von HRID 1789758
[CH3:1][S-:2].[Na+].Cl[C:5]1[C:10]([O:11][CH2:12][CH2:13][OH:14])=[CH:9][CH:8]=[CH:7][N:6]=1>CN(C=O)C>[CH3:1][S:2][C:5]1[C:10]([O:11][CH2:12][CH2:13][OH:14])=[CH:9][CH:8]=[CH:7][N:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 4378561Sodium methanethiolateHCID 22036312HCID 22036312, Verbindung

Produkt 1

HCID 220363602-[[2-(Methylthio)-3-pyridinyl]oxy]ethanolAusbeute 37,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a suspension of sodium thiomethoxide (3.01 g, 42.9 mmol) in dry DMF (30 mL) was 2-[(2-chloro-3-pyridinyl)oxy]ethanol (7.82 g, 45.1 mmol, from Example 193, Step 1) added and the reaction mixture was stirred at ambient temperature for 1 h. The solvent was removed under reduced pressure and the residue was partitioned between brine/1 M aqueous NaOH and CHCl3. The aqueous phase was extracted with an additional portion of CHCl3 and the combined organic layers were dried (MgSO4) and concentrated. The resulting red oil was purified by column chromatography on silica using toluene/Et3N/MeOH (96:2:2) as eluent to give 3.0 g (36%) of the title compound as brownish crystals: mp 80° C. Anal. (C7H11, NO2S)C, H, N.

Aufarbeitung

  1. additionadded
  2. customThe solvent was removed under reduced pressure
  3. customthe residue was partitioned between brine/1 M aqueous NaOH and CHCl3
  4. extractionThe aqueous phase was extracted with an additional portion of CHCl3
  5. dry with materialthe combined organic layers were dried (MgSO4)
  6. concentrationconcentrated
  7. customThe resulting red oil was purified by column chromatography on silica

Quellen und Nachweise

ORD-Eintrag
ord-091c8811c9fa4cf69a2d9d1e364959ff
Quelldatensatz
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07071180B2

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