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Water → 3-Methoxymethyl-5-[(4-methylphenyl)-sulfonyl]-1,2,4-thiadiazole

HRID 1416320
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1416320
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:11]#[N:12])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH3:13][O:14][CH2:15][C:16]1OC(=O)[S:18][N:17]=1.O>CCCCCCCCCCCC>[CH3:13][O:14][CH2:15][C:16]1[N:12]=[C:11]([S:8]([C:5]2[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][CH:6]=2)(=[O:10])=[O:9])[S:18][N:17]=1
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Komponenten

5

Edukt 3

HCID 962WaterHCID 87946p-Toluenesulphonyl cyanideHCID 218503335-Methoxymethyl-1,3,4-oxathiazol-2-one

Produkt 1

HCID 218503733-Methoxymethyl-5-[(4-methylphenyl)-sulfonyl]-1,2,4-thiadiazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8182DodecaneLösungsmittel

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

4-Methylbenzenesulfonyl cyanide (16.26 g) was added to an emulsion of 5-methoxymethyl-1,3,4-oxathiazol-2-one (6.6 g) in dodecane (60 cm3). The reaction mixture was stirred and heated at 150° C. for 18 hours, then cooled. Water was added and the product extracted into ethyl acetate. The combined organic phases were dried (MgSO4) and ethyl acetate was removed by evaporation under reduced pressure. The residue separated into a brown liquid and a clear dodecane layer which was removed and discarded. Chromatography of the brown liquid on silica gel (Sorbsil C30) using 3:7 ethyl acetate:hexane as eluant give a pale orange oil which solidified on standing (6.94 g). M+ =284; 1H NMR: δ 2.40(3H,s); 3.45(3H,s); 4.7(2H,s); 7.4(2H,d); 8.0(2H,d); (mp 43.4-45-4° C.).

Aufarbeitung

  1. temperaturecooled
  2. extractionthe product extracted into ethyl acetate
  3. dry with materialThe combined organic phases were dried (MgSO4) and ethyl acetate
  4. customwas removed by evaporation under reduced pressure
  5. customThe residue separated into a brown liquid
  6. customa clear dodecane layer which was removed
  7. customhexane as eluant give a pale orange oil which
  8. custom(mp 43.4-45-4° C.)

Quellen und Nachweise

ORD-Eintrag
ord-1870628798e8491aad2820e66a60204b
Quelldatensatz
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05912243

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