1,2-Ethanediamine, 4-methylbenzenesulfonate (1:?) → p-Toluenesulfonic acid

HRID 66768

Reaktionsgleichung

Reaktionsgleichung von HRID 66768
CC1C=CC(SCC#N)=CC=1.[C:12]1([CH3:22])[CH:17]=[CH:16][C:15]([S:18]([OH:21])(=[O:20])=[O:19])=[CH:14][CH:13]=1.C(N)CN>ClC1C=CC=CC=1Cl.C(Cl)Cl>[CH3:22][C:12]1[CH:17]=[CH:16][C:15]([S:18]([OH:21])(=[O:20])=[O:19])=[CH:14][CH:13]=1

Komponenten

5

Edukt 2

HCID 2250301,2-Ethanediamine, 4-methylbenzenesulfonate (1:?)HCID 27997712-[(4-Methylphenyl)thio]acetonitrile

Produkt 1

HCID 6101p-Toluenesulfonic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittelHCID 72391,2-DichlorobenzeneLösungsmittel

Versuchsvorschrift

A mixture of 27 g of 4-methylthiophenoxyacetonitrile and 35 g of ethylenediamine p-toluenesulfonate in 50 ml of 1,2-dichlorobenzene was heated at 158°-180° C. for about 45 minutes. The reaction mixture was cooled, diluted with CH2Cl2 and filtered to obtain the p-toluenesulfonate salt. After washing with CH2Cl2, the p-toluenesulfonate salt was slurried with water and then 40 ml of an aqueous 5 normal (N) sodium hydroxide solution added to the slurry. Extracting the mixture with CH2Cl2 and then evaporating the CH2Cl2 left 30 g of the free base. The free base was heated in cyclohexane/methylchloroform, the resulting mixture was then cooled and the solids removed by filtration. The free base was then dissolved in 150 ml of isopropanol and acidified with hydrochloric acid (HCl) in isopropanol to give the hydrochloride salt (31 g). The 2-((4-(methylthio)phenoxy)methyl)-2-imidazoline hydrochloride was found to have a m.p. of 190°-191° C.

Aufarbeitung

  1. temperaturewas heated at 158°-180° C. for about 45 minutes
  2. temperatureThe reaction mixture was cooled
  3. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-a440dca77bc945aeab5a44eccc4bab0c
Quelldatensatz
uspto-grants-1982_08
Patentnummer
US04343808

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