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Phosphorus oxychloride → 4-Chloro-2-ethylthieno(3,2-d)pyrimidine

HRID 478066
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 478066
[CH2:1]([C:3]1[N:4]=[C:5](O)[C:6]2[S:11][CH:10]=[CH:9][C:7]=2[N:8]=1)[CH3:2].P(Cl)(Cl)([Cl:15])=O>>[Cl:15][C:5]1[C:6]2[S:11][CH:10]=[CH:9][C:7]=2[N:8]=[C:3]([CH2:1][CH3:2])[N:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 178437764HCID 178437764, Verbindung

Produkt 1

HCID 107031404-Chloro-2-ethylthieno(3,2-d)pyrimidine

Versuchsvorschrift

2-Ethyl-4-hydroxythieno[3,2-d]pyrimidine (0.6725 g, 0.00373M) was refluxed with phosphorus oxychloride (20 ml) for 2 hours. The reaction mixture was cooled, concentrated under vacuum, the residue dissolved in methylene chloride, poured over ice and water and basified with ammonia. The layers were separated and the aqueous layer extracted with ether. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated under vacuum to obtain the product, 0.65 g, as a tan solid, m.p. 46°-48° C. the structure of which was confirmed by NMR.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled
  2. concentrationconcentrated under vacuum
  3. dissolutionthe residue dissolved in methylene chloride
  • additionpoured over ice and water and basified with ammonia
  • customThe layers were separated
  • extractionthe aqueous layer extracted with ether
  • washThe combined organic extracts were washed with brine
  • dry with materialdried (MgSO4)
  • concentrationconcentrated under vacuum
  • customto obtain the product, 0.65 g
  • Quellen und Nachweise

    ORD-Eintrag
    ord-586c38cf10a64d378fa2584155ead93b
    Quelldatensatz
    uspto-grants-1989_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04889856

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