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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 232723Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/232723

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktEthyl isopropylcarbamateHCID 17433—
EduktSulfur dichlorideHCID 25353—
LösungsmittelDichloromethaneHCID 6344—
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 ml 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 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 hexane resulted 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
PatentnummerUS05591764
Quelldatensatzuspto-grants-1997_01
ORD IDord-2a23b4242a5f4f5f9d5abfbbd60b95d4
Quellennotizuspto-grants-1997_01