3-(Dimethylamino)-1-propanol → N,N1-Dimethyl-S-(3-dimethylaminopropyl)isothiourea
Reaction equation
[CH3:1][N:2]([CH3:7])[CH2:3][CH2:4][CH2:5]O.[CH3:8][N:9]([CH3:13])[C:10]([NH2:12])=[S:11]>Br>[CH3:8][N:9]([CH3:13])[C:10](=[NH:12])[S:11][CH2:5][CH2:4][CH2:3][N:2]([CH3:7])[CH3:1]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3-dimethylaminopropanol (10.3 g), N,N1 -dimethylthiourea (10.4 g) and aqueous hydrobromic acid (48%, 60 ml) was boiled under reflux for 18 hours and evaporated to dryness. The residue was recrystallised from ethanol to give the dihydrobromide of the title compound m.p. 173°-174°.
Workup
- temperatureunder reflux for 18 hours
- customevaporated to dryness
- customThe residue was recrystallised from ethanol
Sources & evidence
- ORD record
- ord-761a148bb78d41729bb09765b10f2090
- Source dataset
- uspto-grants-1983_03
- Patent number
- US04378365
Reaction notes
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