HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614150Generated: October 25, 2026
Pyridine → Ethyl (chlorosulfenyl)(1-methylethyl)carbamate
https://huagongshe.com/reaction/1614150
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl isopropylcarbamate | HCID 17433 | — |
| Reactant | Sulfur dichloride | HCID 25353 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl (chlorosulfenyl)(1-methylethyl)carbamate | HCID 20139494 | 63.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05196408 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-65e79821a2a64cf883fb2de8e5d95798 |
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| Source note | uspto-grants-1993_03 |
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