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HRID 894331作成日:2026年10月25日

1,1,2,2-Tetrachloroethylsulfenyl chloride → N-methoxycarbonylmethyl-N-(1,1,2,2-tetrachloroethylthio)cyclohexanesulfonamide

https://huagongshe.com/reaction/894331

反応式

関与物質

役割名称HCID仕込み量
反応物1,1,2,2-Tetrachloroethylsulfenyl chlorideHCID 14453—
反応物Sodium HydroxideHCID 14798—
反応物N-(methoxycarbonylmethyl)cyclohexanesulfonamideHCID 20575296—
触媒Benzyl triethylammonium chlorideHCID 66133—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-methoxycarbonylmethyl-N-(1,1,2,2-tetrachloroethylthio)cyclohexanesulfonamideHCID 2057529019.2%

反応条件

温度25 °C

反応手順

A 1.2 g (0.03 mol) sample of sodium hydroxide in 1.2 ml water was added dropwise to a solution of 6.5 g (0.03 mol) N-(methoxycarbonylmethyl)cyclohexanesulfonamide, 7.0 g (0.03 mol) 1,1,2,2-tetrachloroethylsulfenyl chloride, 0.5 g. triethylbenzylammonium chloride in 100 ml dichloromethane. The resulting reaction mixture was stirred at about 25° C. for 3 hours, washed with water, dried over magnesium sulfate and evaporated under reduced pressure to give an oil residue. The residue was chromatographed through silica gel. Elution with 10% ethyl ether/hexane gave 2.5 g of the product as an oil. Elemental analysis for C11H17Cl4NO4S2 showed: %Cl, calc. 32.7, found 32; %S, calc. 14.8, found 15.1. The product is tabulated in Table I as Compound No. 2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04283416
出典データセットuspto-grants-1981_08
ORD IDord-c6cf0941349d4d11b21b78696bc1c7b0
出典メモuspto-grants-1981_08