Water → HCID 22758373, Verbindung

HRID 1415273Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1415273
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]2[S:16](=[O:18])(=[O:17])[CH2:15][CH2:14][CH2:13][S:12]2(=[O:20])=[O:19])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[H-].[Na+].[CH2:23]([CH:25]1[O:27][CH2:26]1)Cl.O>CN(C)C=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11]2([CH2:23][CH:25]3[O:27][CH2:26]3)[S:12](=[O:19])(=[O:20])[CH2:13][CH2:14][CH2:15][S:16]2(=[O:17])=[O:18])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]

Komponenten

6

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

9.6 of 2-(3,4-dimethoxyphenyl)-m-dithiane-1,1,3,3-tetraoxide (prepared as described in Example 2) are dissolved in 35 ml of dimethylformamide and, with stirring under argon, treated with 1.2 g of sodium hydride at room temperature. The suspension is stirred at 40° C for a further 0.5 hour, then cooled and treated with 2.8 g of epichlorohydrin. The mixture is then heated at 100° C for 16 hours. After cooling to room temperature, the suspension is poured on to water and the oily material extracted with chloroform. After evaporation of the solvent, the residue is chromatographed on silica gel with chloroform/ethanol (98:2). The 2-(3,4-dimethoxyphenyl)-2-(2,3-epoxypropyl)-m-dithiane-1,1,3,3-tetraoxide obtained is recrystallized from methylene chloride/ethanol and has a melting point of 175°-176° C.

Aufarbeitung

  1. stirringThe suspension is stirred at 40° C for a further 0.5 hour
  2. temperaturecooled
  3. temperatureAfter cooling to room temperature
  4. extractionthe oily material extracted with chloroform
  5. customAfter evaporation of the solvent
  6. customthe residue is chromatographed on silica gel with chloroform/ethanol (98:2)

Quellen und Nachweise

ORD-Eintrag
ord-2397f723f52d4b0c94f99ba91fac1989
Quelldatensatz
uspto-grants-1977_01
Patentnummer
US04003914

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