Trimethylamine → 2-[(2-Aminoethoxyhydroxyphosphinyl)oxy]-N,N,N-trimethylethanaminium hydroxide

HRID 1449428Notes

Reaction equation

HRID 1449428 reaction equation
[NH2:1][CH2:2][CH2:3][O:4][P:5]1(=[O:10])[O:9]C[CH2:7][O:6]1.[CH3:11][N:12]([CH3:14])[CH3:13].[C:15](#N)C>>[OH-:4].[NH2:1][CH2:2][CH2:3][O:4][P:5]([OH:10])([O:6][CH2:7][CH2:11][N+:12]([CH3:15])([CH3:14])[CH3:13])=[O:9]

Participants

4

Procedure

2-(2-aminoethoxy)-2-oxo-1,3,2-dioxaphospholane was dissolved in acetonitrile (20 ml) and added to trimethylamine (14.3 ml) in a glass pressure bottle stored in liquid nitrogen. The pressure bottle was closed, allowed to warm to ambient temperature over 0.5 hour and was then warmed to 60° C. for 16 hours. A pale yellow gum was deposited during this time. Excess trimethylamine was bubbled off and the supernatant decanted. The gum was dissolved in methanol, preabsorbed onto silica gel and purified by chromatography on silica gel eluting with methanol and methanol/25% aqueous ammonia mixtures. 2-[(2-Aminoethoxyhydroxyphosphinyl)oxy]-N,N,N-trimethylethanaminium hydroxide, inner salt was obtained as a pale yellow foam.

Workup

  1. customThe pressure bottle was closed
  2. temperaturewas then warmed to 60° C. for 16 hours
  3. customExcess trimethylamine was bubbled off
  4. dissolutionThe gum was dissolved in methanol
  5. custompreabsorbed onto silica gel
  6. custompurified by chromatography on silica gel eluting with methanol and methanol/25% aqueous ammonia mixtures

Sources & evidence

ORD record
ord-93c9835b077d4c5e996b8ded008f908b
Source dataset
uspto-grants-1997_02
Patent number
US05599587

Reaction notes

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