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2-Mercaptoethanol → 2-[(2-Pyridin-4-ylethyl)thio]ethanol

HRID 1389801
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1389801
C[O-].[Na+].[SH:4][CH2:5][CH2:6][OH:7].[CH:8]([C:10]1[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=1)=[CH2:9]>C(O)C>[OH:7][CH2:6][CH2:5][S:4][CH2:9][CH2:8][C:10]1[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 15672-MercaptoethanolHCID 75024-VinylpyridineHCID 10942334Sodium Methoxide

Produkt 1

HCID 20584062-[(2-Pyridin-4-ylethyl)thio]ethanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel3×

Versuchsvorschrift

Under a nitrogen atmosphere, sodium methoxide (1.62 g., 0.03 mole) was dissolved in 36 ml. of stirring absolute ethanol and the solution cooled in an ice bath. 2-Mercaptoethanol (2.34 g., 0.03 mole) in 6 ml. of absolute ethanol was added over approximately 5 minutes. Finally, 4-vinylpyridine (3.22 g., 0.03 mole) in approximately 20 ml. of absolute ethanol was added over 15 minutes. The reaction mixture was allowed to warm to room temperature and stirred for 23 hours. The reaction mixture was concentrated to a thick oil (7.28 g.). The oil was diluted with a small amount of chloroform (a strong exotherm occurred, leading to refluxing of the chloroform) and chromatographed on silica gel, with large volumes of chloroform and finally chloroform/1% methanol as eluant. Product containing fractions (from the latter eluant) were combined and evaporated to yield the free base of 4-[2-(2-hydroxyethylthio)ethyl]pyridine [2.49 g.; oil; m/e calcd.: 183, found: 183; ir (film): 3.10, 3.45, 3.52, 6.23, 7.07, 9.40, 9.57, 9.98 and 12.44μ; pnmr/CDCl3 /TMS/δ: 8.53 (m, 2H), 7.17 (m, 2H), 3.77 (t, 2H), 3.57 (s, 1H, exchanges with D2O), 2.85 (m, 4H) and 2.73 ppm (t, 2H)].

Aufarbeitung

  1. temperaturethe solution cooled in an ice bath
  2. concentrationThe reaction mixture was concentrated to a thick oil (7.28 g.)
  3. additionThe oil was diluted with a small amount of chloroform (a strong exotherm
  4. temperatureto refluxing of the chloroform) and
  5. customchromatographed on silica gel, with large volumes of chloroform and finally chloroform/1% methanol as eluant
  6. additionProduct containing fractions (from the latter eluant)
  7. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-13b70061753f4a89be0102c5618fb7c9
Quelldatensatz
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04246263

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