1,1,2,2-Tetrachloroethylsulfenyl chloride → HCID 20575290, Verbindung

HRID 904346Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 904346
[OH-].[Na+].[CH3:3][O:4][C:5]([CH2:7][NH:8][S:9]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)(=[O:11])=[O:10])=[O:6].[Cl:18][C:19]([Cl:25])([S:23]Cl)[CH:20]([Cl:22])[Cl:21]>O.[Cl-].C([N+](CC)(CC)CC1C=CC=CC=1)C.ClCCl>[CH3:3][O:4][C:5]([CH2:7][N:8]([S:23][C:19]([Cl:25])([Cl:18])[CH:20]([Cl:22])[Cl:21])[S:9]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)(=[O:10])=[O:11])=[O:6]

Komponenten

7

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

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.

Aufarbeitung

  1. customThe resulting reaction mixture
  2. washwashed with water
  3. dry with materialdried over magnesium sulfate
  4. customevaporated under reduced pressure
  5. customto give an oil residue
  6. customThe residue was chromatographed through silica gel
  7. washElution with 10% ethyl ether/hexane

Quellen und Nachweise

ORD-Eintrag
ord-5caf51a52b2143258a8e055037917d65
Quelldatensatz
uspto-grants-1980_10
Patentnummer
US04230875

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