Water → HCID 54409492, Verbindung

HRID 1701159Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1701159
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][C:11]([CH:14](Cl)[CH3:15])=[CH:10][CH:9]=1.[CH3:17][O:18][C:19](=[O:22])[CH2:20][SH:21].C(=O)([O-])[O-].[K+].[K+].O>CS(C)=O>[CH3:17][O:18][C:19](=[O:22])[CH2:20][S:21][CH:14]([C:11]1[CH:12]=[CH:13][C:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[Cl:1])=[CH:9][CH:10]=1)[CH3:15]

Komponenten

6

Versuchsvorschrift

294 gm (1.17 mol) of 1-(2'-chloro-4-biphenylyl)-1-chloro-ethane and 149.2 gm (1.4 mol) of thioglycolic acid methyl ester were dissolved in 1 liter of dimethyl sulfoxide, and 194.3 gm (1.4 mol) of potassium carbonate were added to the solution in small portions, while stirring vigorously and cooling on ice water. After stirring the mixture for 4 hours, 3 liters of water were added. The reaction product was extracted with toluene, and after washing the extract with water and drying it over magnesium sulfate, the solvent was removed in vacuo. Yield: 359:0 gm (95.5% of theory). Rf -value: 0.6 on carrier 1 with cyclohexane/ethyl acetate=4:1.

Aufarbeitung

  1. temperaturecooling on ice water
  2. stirringAfter stirring the mixture for 4 hours
  3. extractionThe reaction product was extracted with toluene
  4. washafter washing the
  5. extractionextract with water
  6. dry with materialdrying it over magnesium sulfate
  7. customthe solvent was removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-5267a385b5024a53a0e3dd8cca1bd5f2
Quelldatensatz
uspto-grants-1980_03
Patentnummer
US04191776

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