chloro-(4-chlorobutyl)-dimethylsilane

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

Procedure: In a 500 ml glass reactor fitted with a mechanically driven stirrer, thermometer, nitrogen inlet, dropping funnel and water-cooled reflux condenser was charged 7.9 g magnesium chip. Via the dropping funnel was added a solution of 47.5 g 4-chlorobenzyl chloride in 200 ml diethyl ether with stirring over a period of 1/2 an hour. After the addition was complete, the reaction was refluxed for 1/2 hour, then cooled to room temperature. To the Grignard reagent was added a solution of 31.0 g chlorodimethyl-4-chloro-n-butylsilane (Petrarch Systems Inc., Bristol, PA) in 50 ml ether. The reaction mixture was refluxed for 1 hour after the addition was complete, then cooled to room temperature. A solution of 10 g citric acid in 200 ml water was added to hydrolyze the reaction. The organic layer was separated, dried over magnesium sulfate and the solvent removed at room temperature under vacuum. Low boiling impurities were removed by distillation at 150° C. under 15 mm vacuum. The residue was a yellow oil. Vapor phase chromatography showed the compound to be about 95 percent pure. Its NMR spectrum was consistent with the expected compound. In a 500 ml glass reactor fitted with a mechanically driven stirrer thermometer, nitrogen inlet, dropping reflux condenser After the addition the reaction was refluxed for 1/2 hour The reaction mixture was refluxed for 1 hour after the addition cooled to room temperature the reaction The organic layer was separated dried over magnesium sulfate the solvent removed at room temperature under vacuum were removed by distillation at 150° C. under 15 mm vacuum