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Hexane → N-(Diphenoxymethylene)-methanesulfonamide

HRID 2351010
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2351010
[C:1]([O:4][CH2:5][CH3:6])(=[O:3])C.[CH3:7][S:8]([NH2:11])(=[O:10])=[O:9].[CH3:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]>>[CH3:7][S:8]([N:11]=[C:1]([O:4][C:5]1[CH:6]=[CH:15][CH:14]=[CH:13][CH:12]=1)[O:3][C:14]1[CH:13]=[CH:12][CH:17]=[CH:16][CH:15]=1)(=[O:10])=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 8058HexaneHCID 8857Ethyl AcetateHCID 72879Methanesulfonamide

Produkt 1

HCID 13738851N-(Diphenoxymethylene)-methanesulfonamideAusbeute 49 %

Versuchsvorschrift

267 g of diphenyl carbonate and 298 g of phosphorus pentachloride were reacted at 160° C. for 15 hours with distilling off the phosphorus oxychloride generated by the reaction. After the completion of the reaction, phosphorus oxychloride and residual phosphorus pentachloride were removed by distillation under reduced pressure to obtain dichloro-diphenoxymethane. Thereto were added 600 ml of anhydrous ethyl acetate and 148 g of methanesulfonamide, and the mixture was refluxed for 8 hours. After cooling, 1 liter of n-hexane was added to the mixture and the crystals deposited were collected by filtration. The crystals were washed with water and dried to obtain 179 g (yield: 49%) of diphenyl methanesulfonylimidocarbonate having a melting point of 124°-125.5° C.

Aufarbeitung

  1. temperaturethe mixture was refluxed for 8 hours
  2. temperatureAfter cooling
  3. filtrationthe crystals deposited were collected by filtration
  4. washThe crystals were washed with water
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-1f9ab6f11c464734bc710c8093a4fcff
Quelldatensatz
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04871765

Notizen zur Reaktion

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