戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 232723作成日:2026年10月25日

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

https://huagongshe.com/reaction/232723

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Ethyl isopropylcarbamateHCID 17433—
反応物Sulfur dichlorideHCID 25353—
溶媒DichloromethaneHCID 6344—
生成物Ethyl (chlorosulfenyl)(1-methylethyl)carbamateHCID 2013949463.2%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05591764
出典データセットuspto-grants-1997_01
ORD IDord-2a23b4242a5f4f5f9d5abfbbd60b95d4
出典メモuspto-grants-1997_01