Hydrochloric Acid → HCID 12717840, compound
Reaction equation
[ClH:1].[CH3:2][N:3]([CH2:5][P:6](=[O:15])([CH2:11][N:12]([CH3:14])[CH3:13])[CH2:7][N:8]([CH3:10])[CH3:9])[CH3:4]>O>[ClH:1].[ClH:1].[ClH:1].[CH3:10][N:8]([CH2:7][P:6](=[O:15])([CH2:11][N:12]([CH3:14])[CH3:13])[CH2:5][N:3]([CH3:2])[CH3:4])[CH3:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Five ml (0.03 mol) of a 6 N hydrochloric acid solution was pipetted into a stoppered flask containing 2.21 g (0.01 mol) of tris(dimethylaminomethyl)phosphine oxide. The mixture was shaken until the fuming and exotherming subsided, allowed to stand 30 min, and then stripped of water under vacuum, leaving 3.32 g (100% yield) of tris(dimethylaminomethyl)phosphine oxide trihydrochloride as a white, crystalline solid, m.p. 228°-229° C. dec.
Sources & evidence
- ORD record
- ord-d6e5264171014faa91fbc3c87526e23d
- Source dataset
- uspto-grants-1980_12
- Patent number
- US04239701
Reaction notes
Loading…