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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2396079Erstellt: 25. Oktober 2026

Chloride → Ethyl (chlorosulfenyl)(1-methylethyl)carbamate

https://huagongshe.com/reaction/2396079

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorideHCID 312—
EduktEthyl isopropylcarbamateHCID 17433—
EduktSulfur dichlorideHCID 25353—
LösungsmittelPyridineHCID 1049—
ProduktEthyl (chlorosulfenyl)(1-methylethyl)carbamateHCID 2013949463,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of ethyl (1-methylethyl)carbamate (13.1 g, 0.1 mol) in 100 mlmethylene chloride cooled to 0° C. was added sulfur dichloride (11.3g, 0.11 mol) in one portion. While maintaining the temperature of the mixture at 0° C., pyridine (8.7 g, 0.11 mol) was added dropwise over eleven minutes. After complete addition of the pyridine the temperature was allowed to rise to room temperature and stirring was continued for additional 1.5 hours. The mixture was let stand overnight. Methylene chloride was evaporated under vacuum and 100 ml hexane was added. Filteration of the pyridine hydrochloride and evaporation of hexaneresulted in an orange oil which was distilled in a Kugelrohr apparatus to give 12.5 g of the title compound Bp: 64°-80° (bath temperature) at 1.4 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05491162
Quelldatensatzuspto-grants-1996_02
ORD IDord-e8f9e27215db4393b9936f94e2f452b6
Quellennotizuspto-grants-1996_02