Thionyl Chloride → HCID 178458779, Verbindung

HRID 2236538Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2236538
O[CH2:2][C:3]1[CH:8]=[C:7]([OH:9])[C:6]([O:10][CH2:11][CH2:12][CH3:13])=[CH:5][N:4]=1.S(Cl)([Cl:16])=O>C(Cl)(Cl)Cl>[Cl:16][CH2:2][C:3]1[CH:8]=[C:7]([OH:9])[C:6]([O:10][CH2:11][CH2:12][CH3:13])=[CH:5][N:4]=1

Komponenten

4

Versuchsvorschrift

To a mixture of 2-hydroxymethyl-5-propoxy-pyridin-4-ol (5.56 g, 30.3 mmole) and 30 mL of chloroform stirred cooled with an ice bath is added 30 mL of thionyl chloride (x g, 0.x mole). This is stirred for 15 minutes at ice bath temperature and then refluxed for 1 hour. The reaction mixture is cooled, evaporated to dryness in vacuo and then treated with isopropanol. The solid is filtered, washed with fresh isopropanol, then ether and air dried to give an off-white solid, 3.4 g, (48%), m.p. 165-7° C.; MS (ES+): m/z 202.3 (M+H).

Aufarbeitung

  1. temperaturecooled with an ice bath
  2. stirringThis is stirred for 15 minutes at ice bath temperature
  3. temperaturerefluxed for 1 hour
  4. temperatureThe reaction mixture is cooled
  5. customevaporated to dryness in vacuo
  6. additiontreated with isopropanol
  7. filtrationThe solid is filtered
  8. washwashed with fresh isopropanol
  9. dry with materialether and air dried
  10. customto give an off-white solid, 3.4 g, (48%), m.p. 165-7° C.

Quellen und Nachweise

ORD-Eintrag
ord-66f1ec9bb0884da8a56ede6feae45b90
Quelldatensatz
uspto-grants-2010_05
Patentnummer
US07713994B2

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