Reaction equation
Cl.[Cl:2][CH2:3][CH2:4][CH2:5][N:6]([CH2:11][CH2:12][CH2:13][CH3:14])[CH2:7][CH2:8][CH2:9][CH3:10].N>>[Cl:2][CH2:3][CH2:4][CH2:5][N:6]([CH2:11][CH2:12][CH2:13][CH3:14])[CH2:7][CH2:8][CH2:9][CH3:10]Participants
3
Procedure
18.6 g of 68.4% 1-chloro-3-(di-n-butylamino)-propane hydrochloride (52.6 mmol) are placed in an equipped reactor and then 9.97 g of a 20% aqueous ammonia solution (56.9 mmol) are added at 20° C. The mixture is stirred for 15 minutes, and then the phases are decanted off and separated: the bottom phase consists of 1-chloro-3-(di-n-butylamino)-propane in the form of a free base. This phase is washed with 10 ml of water and 9.99 g of 1-chloro-3-(di-n-butylamino)-propane are thus isolated.
Workup
- customthe phases are decanted off
- customseparated
- washThis phase is washed with 10 ml of water and 9.99 g of 1-chloro-3-(di-n-butylamino)-propane
- customare thus isolated
Sources & evidence
- ORD record
- ord-1dd0129deb514f2fb01b0b8780a614c3
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08871956B2
Linked notes
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