[CH2:1]([NH:4][CH2:5][CH2:6]CO)[CH2:2][CH3:3].[CH:9]([Cl:12])(Cl)[Cl:10]>S(Cl)(Cl)=O>[ClH:10].[CH2:1]([NH:4][CH2:5][CH2:6][CH2:9][Cl:12])[CH2:2][CH3:3]There was added to about 124 parts of the above N-propyl-3-amino propanol dissolved in 1194 parts of chloroform under an atmosphere of nitrogen and at a temperature of about 0° C., 189 parts of thionyl chloride at a rate which was sufficient to maintain the temperature of the resulting reaction mixture below 20° C. When the addition was complete, the solution was brought to reflux for 30 minutes. The reaction mixture was then quenched with excess ethanol and concentrated to provide a yellow viscous oil. There was obtained a quantitative yield of N-propylamino-3-chloro propane hydrochloride after the aforementioned yellow viscous oil was crystallized from ethanol in the form of a white crystalline solid; (M.P. 246°-247° C.).
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