phenyl benzenesulfonate

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: All apparatus is rigorously dried and flushed with nitrogen before use. The reaction is performed in a 25 ml flask equipped with a magnetic stirring bar and a calcium chloride drying tube. The flask is charged with benzenesulfonyl chloride (11.60 g, 65.7 mmol), phenol (5.60 g, 59.6 mmol), and 4-dimethylaminopyridine (0.36 g, 2.98 mmol), and anhydrous pyridine (20 ml). The reaction mixture is stirred and heated at reflux, and the progress of the reaction is monitored by high performance liquid chromatography. At the conclusion of the reaction, the mixture is cooled and quenched with water (25 ml), extracted with ether (50 ml), and washed successively with 50 ml portions of water, 5% sodium hydroxide (2×), water, and brine. The organic phase is then dried over magnesium sulphate, filtered, and concentrated to yield 13.1 g (94%) of the crude product as a yellow oil. This product is further purified by distillation on a Kugelrohr apparatus under vacuum to give 11.3 g (81%) of the product as a colorless oil. The oxidative stability of the product is determined by pressure differential scanning calorimetry (PDSC). The results are reported below in Table 1. All apparatus is rigorously dried flushed with nitrogen before use The reaction is performed in a 25 ml flask equipped with a magnetic stirring bar and a calcium chloride drying tube heated at reflux At the conclusion of the reaction the mixture is cooled quenched with water (25 ml) extracted with ether (50 ml) washed successively with 50 ml portions of water, 5% sodium hydroxide (2×), water, and brine The organic phase is then dried over magnesium sulphate filtered concentrated to yield 13.1 g (94%) of the crude product as a yellow oil This product is further purified by distillation on a Kugelrohr apparatus under vacuum