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Water → N-methyl-N-methylthio-N'-(3,4-dichlorophenyl)-urea

HRID 442285
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 442285
[CH3:1][S:2]Cl.C(OCC)C.[CH3:9][NH:10][C:11]([NH:13][C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([Cl:21])[CH:15]=1)=[O:12].O>N1C=CC=CC=1>[CH3:9][N:10]([S:2][CH3:1])[C:11]([NH:13][C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([Cl:21])[CH:15]=1)=[O:12]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 3283Diethyl EtherHCID 19113MonomethyldiuronHCID 138595Methanesulfenylchloride

Produkt 1

HCID 21414094N-methyl-N-methylthio-N'-(3,4-dichlorophenyl)-urea

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Reaktionsbedingungen

Temperatur
-30 °C

Versuchsvorschrift

A mixture of 20 ml of methylsulfenyl chloride and 200ml of ethyl ether was added slowly while keeping the temperature below -30° C. to a solution of 40 g of N-methyl-N'-(3,4-dichlorophenyl)-urea in 500 ml of pyridine and the mixture was stirred for 1 hour at -30° C. After letting the temperature rise to 5° C., the mixture was stirred for 17 hours and the mixture was poured into a mixture of ice and water. The mixture was extracted with methylene chloride and the methylene chloride extract was washed with water and dried. The volatile fractions were removed by distillation under reduced pressure and the residue was crystallized from isopropyl ether to obtain 29.4 g of N-methyl-N-methylthio-N'-(3,4-dichlorophenyl)-urea melting at 93° C. A microanalytical sample was obtained by chromatography over silica gel and elution with a 9-1 benzene-ethyl acetate mixture.

Aufarbeitung

  1. additionwas added slowly
  2. customthe temperature below -30° C.
  3. customto 5° C.
  4. stirringthe mixture was stirred for 17 hours
  5. extractionThe mixture was extracted with methylene chloride
  6. extractionthe methylene chloride extract
  7. washwas washed with water
  8. customdried
  9. customThe volatile fractions were removed by distillation under reduced pressure
  10. customthe residue was crystallized from isopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-1039c6c240cd4c9db0d30ab1815fd8bd
Quelldatensatz
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04045209

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