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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2396085Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2396085

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
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 mlof methylene chloride cooled to 0° C. was added sulfur dichloride (11.3 g, 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 dropwiseover 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 pyridine in hydrochloride and evaporation of hexane resulted an orange oil which was distilled in a Kugelrohr apparatus to give 12.5 g of the title Compound B.P.: 64°-80° (bath temp.)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05491162
Quelldatensatzuspto-grants-1996_02
ORD IDord-002621d69baa40069fe0f4bc1383a5e8
Quellennotizuspto-grants-1996_02