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Dimethyl Sulfoxide → HCID 10380396, Verbindung

HRID 465591
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 465591
CS(C)=O.C(Cl)(=O)C(Cl)=O.[N:11]1[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][CH2:18][CH2:19][CH:20]([OH:32])[CH2:21][CH2:22][CH2:23][CH2:24][O:25][CH:26]2[CH2:31][CH2:30][CH2:29][CH2:28][O:27]2)[CH:12]=1>C(Cl)Cl>[N:11]1[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][CH2:18][CH2:19][C:20](=[O:32])[CH2:21][CH2:22][CH2:23][CH2:24][O:25][CH:26]2[CH2:31][CH2:30][CH2:29][CH2:28][O:27]2)[CH:12]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 679Dimethyl SulfoxideHCID 65578Oxalyl chlorideHCID 10335383HCID 10335383, Verbindung

Produkt 1

HCID 10380396HCID 10380396, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

A solution of 1.62 ml (22.73 mmol) of dimethylsulfoxide in 60 ml dry methylene chloride is cooled to -78° and 1.44 ml (16.53 mmol) oxalyl chloride is added dropwise. The mixture is stirred for 0.5 h at -78° and a solution of 1.0 g (3.31 mmol) of 1-(3-pyridyl)-4-hydroxy-8-(2-tetrahydropyranyloxy)-octane [=5-hydroxy-8-(3-pyridyl)-1-(2-tetrahydropyranyloxy)-octane, see example 37] in 15 ml dry methylene chloride is added and the mixture is stirred for 10 min at -78°. The mixture is warmed to -60° and maintained for 15 min at that temperature. The reaction is quenched by the addition of 6.9 ml triethylamine. The cold bath is removed and the mixture allowed to warm to room temperature. The reaction mixture is extracted with 150 ml methylene chloride and washed with saturated sodium bicarbonate solution. The organic phase is dried, filtered, concentrated and chromatographed using 3:2 ethyl acetate/hexane to yield 1-(3-pyridyl)-4-oxo-8-(2-tetrahydropyranyloxy)-octane; NMR (CDCl3): delta 2.6 (t,2H), 2.4 (t,4H).

Aufarbeitung

  1. stirringthe mixture is stirred for 10 min at -78°
  2. temperatureThe mixture is warmed to -60°
  3. temperaturemaintained for 15 min at that temperature
  4. customThe reaction is quenched by the addition of 6.9 ml triethylamine
  5. customThe cold bath is removed
  6. extractionThe reaction mixture is extracted with 150 ml methylene chloride
  7. washwashed with saturated sodium bicarbonate solution
  8. customThe organic phase is dried
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customchromatographed

Quellen und Nachweise

ORD-Eintrag
ord-fc48880154d049faa4b8d9b9a28b8951
Quelldatensatz
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05153214

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