1,2-Dibromoethane → HCID 13650453, Verbindung

HRID 2290751Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2290751
[N:1]1([CH2:6][C:7]([C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)=[O:8])[CH:5]=[N:4][CH:3]=[N:2]1.[CH2:16]1OCCOCCOCCOCCOCCO[CH2:17]1.[OH-].[K+].BrCCBr>C(Cl)Cl>[F:15][C:12]1[CH:13]=[CH:14][C:9]([C:7]([C:6]2([N:1]3[CH:5]=[N:4][CH:3]=[N:2]3)[CH2:17][CH2:16]2)=[O:8])=[CH:10][CH:11]=1

Komponenten

6

Versuchsvorschrift

To a solution of 2-(1H-1,2,4-triazol-1-yl)-4'-fluoroacetophenone (10.24 g, 50 mMole) in methylene chloride (70 ml) was added 18-Crown-6 ether (1 g) (trade mark for 1,4,7,10,13,16-hexaoxacyclooctadecane) and potassium hydroxide (6.1 g, 109 mMole) with stirring. Ten minutes later 1,2-dibromoethane was added (10.3 g, 55 mMole in one batch. Stirring was continued for 18 hours. The mixture was poured into saturated saline solution (100 ml) and the organic phase was separated, washed with water (3×30 ml) and dried over anhydrous magnesium sulphate. Evaporation gave an oil, weight 13.7 g. Purification was carried out by flash column chromatography under slight pressure (2 p.s.i.) on a Merck "Kieselgel 60" (trade mark) 230-400 mesh fractions after collection and evaporation gave a solid, the pure title compound, 2.9 g, m.p. 73°-75° (25% yield).

Aufarbeitung

  1. stirringStirring
  2. customthe organic phase was separated
  3. washwashed with water (3×30 ml)
  4. dry with materialdried over anhydrous magnesium sulphate
  5. customEvaporation
  6. customgave an oil, weight 13.7 g
  7. customPurification
  8. customafter collection and evaporation
  9. customgave a solid

Quellen und Nachweise

ORD-Eintrag
ord-08f38186bbaf4be58f8aa29e8a73f655
Quelldatensatz
uspto-grants-1986_10
Patentnummer
US04618616

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