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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,1,2,2-Tetrachloroethylsulfenyl chloride | HCID 14453 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | N-(methoxycarbonylmethyl)cyclohexanesulfonamide | HCID 20575296 | — |
| 触媒 | Benzyl triethylammonium chloride | HCID 66133 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-methoxycarbonylmethyl-N-(1,1,2,2-tetrachloroethylthio)cyclohexanesulfonamide | HCID 20575290 | 19.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04283416 |
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| 出典データセット | uspto-grants-1981_08 |
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| ORD ID | ord-c6cf0941349d4d11b21b78696bc1c7b0 |
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| 出典メモ | uspto-grants-1981_08 |
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