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Dichloromethane → N-methyl-N-(diethylaminosulfenyl)carbamoyl fluoride

HRID 1447118
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1447118
[FH:1].C(Cl)Cl.[CH3:5][N:6]=[C:7]=[O:8].[CH2:9]([N:11]([CH2:14][CH3:15])[S:12]Cl)[CH3:10]>C(N(CC)CC)C>[CH3:5][N:6]([S:12][N:11]([CH2:14][CH3:15])[CH2:9][CH3:10])[C:7]([F:1])=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6344DichloromethaneHCID 12228Methyl IsocyanateHCID 14917Hydrofluoric AcidHCID 12297776N,N-diethylaminosulfenyl chloride

Produkt 1

HCID 12799217N-methyl-N-(diethylaminosulfenyl)carbamoyl fluorideAusbeute 62,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8471
Triethylamine
Lösungsmittel

Versuchsvorschrift

Anhydrous hydrogen fluoride (3.0 g, 0.15 mole) was added to 150 ml of methylene chloride at -10° C. Then 8.6 g of methylisocyanate was added, followed by 20.9 g (0.15 mole) of N,N-diethylaminosulfenyl chloride at 0° C. Triethylamine (15.2 g) was then added at 0° C. over a 15-minute period, and the mixture was stirred at +5° C. for 1 hour. The mixture was then extracted with water (100 ml), saturated sodium bicarbonate solution, and water again. After drying (MgSO4), the solvent was removed in vacuo, and the crude residue was vacuum distilled to give 17 g of N-methyl-N-(diethylaminosulfenyl)carbamoyl fluoride, b.p. 57° C./0.8 mm (62.9 percent yield).

Aufarbeitung

  1. extractionThe mixture was then extracted with water (100 ml), saturated sodium bicarbonate solution, and water again
  2. dry with materialAfter drying (MgSO4)
  3. customthe solvent was removed in vacuo
  4. distillationdistilled

Quellen und Nachweise

ORD-Eintrag
ord-8eda743ea2b64d51a28c7ad6b49a501c
Quelldatensatz
uspto-grants-1982_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04315928

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