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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614150Generated: October 25, 2026

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

https://huagongshe.com/reaction/1614150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl isopropylcarbamateHCID 17433—
ReactantSulfur dichlorideHCID 25353—
SolventDichloromethaneHCID 6344—
ProductEthyl (chlorosulfenyl)(1-methylethyl)carbamateHCID 2013949463.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196408
Source datasetuspto-grants-1993_03
ORD IDord-65e79821a2a64cf883fb2de8e5d95798
Source noteuspto-grants-1993_03