Reaktion #67502

Reaktionsgleichung

2-cyano-3-fluoro-benzenesulfonyl chloride

thiazolidine

→

2-fluoro-6-(thiazolidine-3-sulfonyl)-benzonitrile

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenThe reaction mixture is concentrated in vacuo
2. 2
   SonstigePurification by Flash chromatography (eluent: cyclohexane/ethyl acetate 1:1)
3. 3
   Waschenby acidic washing with a 1M HCl solution

Vorschrift

440 mg of 2-cyano-3-fluoro-benzenesulfonyl chloride in 10 ml of tetrahydrofuran are treated with 0.36 ml of thiazolidine and the mixture is stirred for 16 hours at room temperature. The reaction mixture is concentrated in vacuo. Purification by Flash chromatography (eluent: cyclohexane/ethyl acetate 1:1) followed by acidic washing with a 1M HCl solution affords 318 mg of 2-fluoro-6-(thiazolidine-3-sulfonyl)-benzonitrile.

Quelle