4-(3-chloropropyl)benzenesulfonyl chloride

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

Procedure: At room temperature, a solution of 10b (12.7 g; 5.0 mmol) in diethyl ether (75 ml) was added dropwise over a period of 2.5 h to a suspension of LiAlH4 (2.9 g; 7.6 mmol) in diethyl ether (50 ml). After the addition had ended, the reaction mixture was stirred at room temperature and with occasional addition of LiAlH4 until no more starting material could be detected by thin-layer chromatography (2.5 h). With ice-cooling, ice was introduced into the reaction mixture, and the aqueous phase was acidified with 10% hydrochloric acid (pH 1). The organic phase was removed and the aqueous phase was extracted with diethyl ether (3×). The combined organic extract was washed with 10% strength aqueous sodium hydroxide solution (4×50 ml) until it was virtually colorless. Dimethyl sulfate (9.0 g; 7.0 mmol) was added to the combined sodium hydroxide extract, and the mixture was stirred at room temperature for 16.5 h. The oily sediment was taken up in diethyl ether. The organic phase was separated off and the aqueous phase was again extracted with diethyl ether (2×). The combined organic extract was dried over Na2SO4 and concentrated. The brown oily residue was subjected to a kugelrohr distillation (0.2 mbar, 250° C.). After the addition could be detected by thin-layer chromatography (2.5 h) With ice-cooling ice was introduced into the reaction mixture The organic phase was removed the aqueous phase was extracted with diethyl ether (3×) The combined organic extract was washed with 10% strength aqueous sodium hydroxide solution (4×50 ml) until it extract The organic phase was separated off the aqueous phase was again extracted with diethyl ether (2×) The combined organic extract was dried over Na2SO4 concentrated The brown oily residue was subjected to a kugelrohr distillation (0.2 mbar, 250° C.)

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

Procedure: At room temperature, a solution of 10b (12.7 g; 5.0 mmol) in diethyl ether (75 ml) was added dropwise over a period of 2.5 h to a suspension of LiAlH4 (2.9 g; 7.6 mmol) in diethyl ether (50 ml). After the addition had ended, the reaction mixture was stirred at room temperature and with occasional addition of LiAlH4 until no more starting material could be detected by thin-layer chromatography (2.5 h). With ice-cooling, ice was introduced into the reaction mixture, and the aqueous phase was acidified with 10% hydrochloric acid (pH 1). The organic phase was removed and the aqueous phase was extracted with diethyl ether (3×). The combined organic extract was washed with 10% strength aqueous sodium hydroxide solution (4×50 ml) until it was virtually colorless. Dimethyl sulfate (9.0 g; 7.0 mmol) was added to the combined sodium hydroxide extract, and the mixture was stirred at room temperature for 16.5 h. The oily sediment was taken up in diethyl ether. The organic phase was separated off and the aqueous phase was again extracted with diethyl ether (2×). The combined organic extract was dried over Na2SO4 and concentrated. The brown oily residue was subjected to a kugelrohr distillation (0.2 mbar, 250° C.). After the addition could be detected by thin-layer chromatography (2.5 h) With ice-cooling ice was introduced into the reaction mixture The organic phase was removed the aqueous phase was extracted with diethyl ether (3×) The combined organic extract was washed with 10% strength aqueous sodium hydroxide solution (4×50 ml) until it extract The organic phase was separated off the aqueous phase was again extracted with diethyl ether (2×) The combined organic extract was dried over Na2SO4 concentrated The brown oily residue was subjected to a kugelrohr distillation (0.2 mbar, 250° C.)

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

Procedure: At room temperature, a solution of 10b (12.7 g; 5.0 mmol) in diethyl ether (75 ml) was added dropwise over a period of 2.5 h to a suspension of LiAlH4 (2.9 g; 7.6 mmol) in diethyl ether (50 ml). After the addition had ended, the reaction mixture was stirred at room temperature and with occasional addition of LiAlH4 until no more starting material could be detected by thin-layer chromatography (2.5 h). With ice-cooling, ice was introduced into the reaction mixture, and the aqueous phase was acidified with 10% hydrochloric acid (pH 1). The organic phase was removed and the aqueous phase was extracted with diethyl ether (3×). The combined organic extract was washed with 10% strength aqueous sodium hydroxide solution (4×50 ml) until it was virtually colorless. Dimethyl sulfate (9.0 g; 7.0 mmol) was added to the combined sodium hydroxide extract, and the mixture was stirred at room temperature for 16.5 h. The oily sediment was taken up in diethyl ether. The organic phase was separated off and the aqueous phase was again extracted with diethyl ether (2×). The combined organic extract was dried over Na2SO4 and concentrated. The brown oily residue was subjected to a kugelrohr distillation (0.2 mbar, 250° C.). After the addition could be detected by thin-layer chromatography (2.5 h) With ice-cooling ice was introduced into the reaction mixture The organic phase was removed the aqueous phase was extracted with diethyl ether (3×) The combined organic extract was washed with 10% strength aqueous sodium hydroxide solution (4×50 ml) until it extract The organic phase was separated off the aqueous phase was again extracted with diethyl ether (2×) The combined organic extract was dried over Na2SO4 concentrated The brown oily residue was subjected to a kugelrohr distillation (0.2 mbar, 250° C.)