Benzyl mercaptan → HCID 13581600, Verbindung

HRID 257137

Reaktionsgleichung

Reaktionsgleichung von HRID 257137
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([N+:11]([O-:13])=[O:12])=[CH:4][C:3]=1[C:14]([F:17])([F:16])[F:15].C(=O)([O-])[O-].[K+].[K+].[CH2:24]([SH:31])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>CN(C)C=O>[CH2:24]([S:31][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([N+:11]([O-:13])=[O:12])=[CH:4][C:3]=1[C:14]([F:17])([F:16])[F:15])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1

Komponenten

5

Edukt 3

HCID 7509Benzyl mercaptanHCID 11430Potassium CarbonateHCID 67851Benzene, 2-chloro-1,5-dinitro-3-(trifluoromethyl)-

Produkt 1

HCID 13581600HCID 13581600, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

67.6 g of 2-chloro-3,5-dinitrobenzotrifluoride are dissolved in 150 ml of N,N-dimethylformamide (DMF) and the mixture is treated with 35.9 g of solid potassium carbonate, treated dropwise with 31 g of benzylmercaptan in 200 ml of DMF with stirring at 0° C., and subsequently stirred for a further 16 hours at room temperature, while cooling.

Aufarbeitung

  1. stirringsubsequently stirred for a further 16 hours at room temperature
  2. temperaturewhile cooling

Quellen und Nachweise

ORD-Eintrag
ord-d6b8c35d48a6424c99ef491dfd6d32b1
Quelldatensatz
uspto-grants-1993_11
Patentnummer
US05260423

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