Thionyl Chloride → HCID 178509690, Verbindung

HRID 35918

Reaktionsgleichung

Reaktionsgleichung von HRID 35918
O[C:2]1([CH:9]([C:15]2[CH:22]=[CH:21][C:18]([C:19]#[N:20])=[CH:17][CH:16]=2)[C:10]2[N:14]=[CH:13][NH:12][N:11]=2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.S(Cl)(Cl)=O>ClCCl>[C:2]1(=[C:9]([C:15]2[CH:22]=[CH:21][C:18]([C:19]#[N:20])=[CH:17][CH:16]=2)[C:10]2[N:14]=[CH:13][NH:12][N:11]=2)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]1

Komponenten

4

Versuchsvorschrift

7 g of crude 4-[1-hydroxycyclohept-1-yl-1(1,2,4-triazolyl)methyl]benzonitrile is dissolved in 50 ml of dichloromethane at 0° and stirred with 20 ml of thionyl chloride for 1 hour at 0°. Then the mixture is concentrated to dryness under an oil pump vacuum, dissolved in 50 ml of dichloromethane, stirred for 2 hours with 30 ml of triethylamine, diluted with water, extracted three times with ethyl acetate, washed with sodium chloride solution, dried over sodium sulfate, concentrated to dryness under vacuum, and chromatographed on silica gel with hexane/ethyl acetate, thus producing 1.9 g of 4-di-cycloheptylidene-1-(1,2,4triazolyl)methyl]benzonitrile as the free base, mp 79°-80°.

Aufarbeitung

  1. concentrationThen the mixture is concentrated to dryness under an oil pump vacuum
  2. dissolutiondissolved in 50 ml of dichloromethane
  3. additiondiluted with water
  4. extractionextracted three times with ethyl acetate
  5. washwashed with sodium chloride solution
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated to dryness under vacuum
  8. customchromatographed on silica gel with hexane/ethyl acetate
  9. customthus producing 1.9 g of 4-di-cycloheptylidene-1-(1,2,4triazolyl)methyl]benzonitrile as the free base, mp 79°-80°

Quellen und Nachweise

ORD-Eintrag
ord-e12fcec478b04c62baf5bd535e7bea4a
Quelldatensatz
uspto-grants-1995_05
Patentnummer
US05411982

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