Water → HCID 13241211, compound
Reaction equation
[CH:1]12[CH2:8][CH:5]([NH:6][NH:7]1)[CH:4]([OH:9])[CH2:3][CH:2]2[OH:10].O>C(O)C.[Ni]>[CH2:8]1[C@H:5]([NH2:6])[C@@H:4]([OH:9])[CH2:3][C@@H:2]([OH:10])[C@@H:1]1[NH2:7]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
6,7-Diaza-bicyclo[3.2.1]octane-2,4-diol (0.20 g) was dissolved in 20 ml. of a mixture of water and ethanol (1:1 by volume) to which was then added 0.2 g of Ranney nickel. The admixture was shaken for 15 hours under an atmosphere of hydrogen at a pressure of 3.4 kg/cm2 for the hydrogenation. The reaction mixture was filtered to remove the catalyst, and the filtrate was concentrated under reduced pressure, giving a crystalline residue. This solid was dispersed in ethanol, removed by filtraton and then dried to afford 0.18 g of 2,5-dideoxystreptamine. Yield 91%. mp. 198°C. This substance was taken up into water, and to the resulting aqueous solution was added a slight excess of 1N hydrochloric acid. The mixture was concentrated by evaporation of the solvent, giving colorless platelets. Recrystallization of this product from water-ethanol gave 2,5-dideoxystreptamine dihydrochloride as colorless platelets of mp. 290°-295°C.
Workup
- filtrationThe reaction mixture was filtered
- customto remove the catalyst
- concentrationthe filtrate was concentrated under reduced pressure
- customgiving a crystalline residue
- customremoved by filtraton
- customdried
Sources & evidence
- ORD record
- ord-8fa35c23e5104c96989e314fd236f6ba
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03959375
Reaction notes
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