HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2396085Erstellt: 25. Oktober 2026
Dichloromethane → Ethyl (chlorosulfenyl)(1-methylethyl)carbamate
https://huagongshe.com/reaction/2396085
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Ethyl isopropylcarbamate | HCID 17433 | — |
| Edukt | Sulfur dichloride | HCID 25353 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | Ethyl (chlorosulfenyl)(1-methylethyl)carbamate | HCID 20139494 | 63,2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05491162 |
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| Quelldatensatz | uspto-grants-1996_02 |
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| ORD ID | ord-002621d69baa40069fe0f4bc1383a5e8 |
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| Quellennotiz | uspto-grants-1996_02 |
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