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Ethyl Acetate → 2-[{2-(1,3-Benzodioxol-5-yl)ethyl}dithio]ethyl nicotinate

HRID 486931
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 486931
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH2:11][S:12][S:13][CH2:14][CH2:15][OH:16])=[CH:9][C:4]=2[O:3][CH2:2]1.Cl.[CH2:18](Cl)[C:19]1[CH:24]=[CH:23][CH:22]=[N:21][CH:20]=1.C(=O)([O-])[OH:27].[Na+].C(OCC)(=O)C>N1C=CC=CC=1.C1C=CC=CC=1>[C:18]([O:16][CH2:15][CH2:14][S:13][S:12][CH2:11][CH2:10][C:8]1[CH:7]=[CH:6][C:5]2[O:1][CH2:2][O:3][C:4]=2[CH:9]=1)(=[O:27])[C:19]1[CH:24]=[CH:23][CH:22]=[N:21][CH:20]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 8857Ethyl AcetateHCID 233943-(Chloromethyl)pyridine hydrochlorideHCID 516892Sodium BicarbonateHCID 190016232-[{2-(1,3-Benzodioxol-5-yl)ethyl}dithio]ethanol

Produkt 1

HCID 190016562-[{2-(1,3-Benzodioxol-5-yl)ethyl}dithio]ethyl nicotinate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 241
Benzene
Lösungsmittel
HCID 1049PyridineLösungsmittel

Versuchsvorschrift

4 g of the 2-[{2-(1,3-benzodioxol-5-yl)ethyl}dithio]ethanol prepared in Example 1 was dissolved in a mixture comprising 20 ml of pyridine and 50 ml of benzene to obtain a solution. 4 g of nicotinyl chloride hydrochloride was added to the solution. The obtained mixture was heated under reflux for 2 hours and poured into ice/water. The obtained mixture was weekly basified with sodium hydrogencarbonate. Ethyl acetate was added to the mixture to carry out the phase separation. The ethyl acetate layer was washed with water five times, dried over anhydrous sodium sulfate and distilled to remove the solvent. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=3:1) to obtain 5.4 g of the title compound as a colorless oil.

Aufarbeitung

  1. customto obtain a solution
  2. temperatureThe obtained mixture was heated
  3. temperatureunder reflux for 2 hours
  4. customthe phase separation
  5. washThe ethyl acetate layer was washed with water five times
  6. dry with materialdried over anhydrous sodium sulfate
  7. distillationdistilled
  8. customto remove the solvent
  9. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=3:1)

Quellen und Nachweise

ORD-Eintrag
ord-da67030f62a24ca6ae691009617a5afd
Quelldatensatz
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05292901

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