Hydrogen Bromide → 6,6-Difluorospermine
Reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][N:5](S(C1C=CC(C)=CC=1)(=O)=O)[CH2:6][C:7]([F:26])([F:25])[CH2:8][CH2:9][N:10](S(C1C=CC(C)=CC=1)(=O)=O)[CH2:11][CH2:12][CH2:13][NH2:14].Br>CC(C)=O>[F:25][C:7]([F:26])([CH2:8][CH2:9][NH:10][CH2:11][CH2:12][CH2:13][NH2:14])[CH2:6][NH:5][CH2:4][CH2:3][CH2:2][NH2:1]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound 1,12-diamino-6,6-difluoro-4,9-di-p-toluenesulfonyl-4,9-diaza-dodecane (2.7 g, 4.36 mM) and 47% aqueous HBr are refluxed (bath temperature: 110° C.) for 17 hours. After cooling to room temperature, the solution is carefully extracted with ether (three times) and finally with chloroform. Evaporation of the aqueous phase, followed by stripping with isopropanol (twice) and ethanol (twice) produces a solid residue which is digested with acetone, collected, and washed with acetone (three times), ethanol (three times) and finally with ether: white crystals, 1.8 g (74%). This material is recrystallized by dissolving in hot (80° C.) aqueous ethanol (100 mL, H2O: ethanol 1:9), filtering through paper, and adding additional ethanol (10-20 mL) to yield the desired 6,6-difluoro-1,12-diamino-4,9-diaza-dodecane as the tetrahydrobromide salt: white crystals 1.2 g, (49%).
Workup
- extractionthe solution is carefully extracted with ether (three times) and finally with chloroform
- customEvaporation of the aqueous phase
- customproduces a solid residue which
- customcollected
- washwashed with acetone (three times), ethanol (three times) and finally with ether
- customThis material is recrystallized
- dissolutionby dissolving in hot (80° C.) aqueous ethanol (100 mL, H2O: ethanol 1:9)
- filtrationfiltering through paper
- additionadding additional ethanol (10-20 mL)
Sources & evidence
- ORD record
- ord-c3b70ee14a914373abfc7f805d065d02
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04778926
Reaction notes
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