Glycidol → N,N,N'-Tri-(2,3-dihydroxypropyl)trimethylenediamine

HRID 1439309Notes

Reaction equation

HRID 1439309 reaction equation
[OH:1][CH:2]([CH2:14][OH:15])[CH2:3][N:4]([CH2:9][CH:10]([OH:13])[CH2:11][OH:12])[CH2:5][CH2:6][CH2:7][NH2:8].[CH2:16]1[O:18][CH:17]1[CH2:19][OH:20]>CO>[OH:1][CH:2]([CH2:14][OH:15])[CH2:3][N:4]([CH2:9][CH:10]([OH:13])[CH2:11][OH:12])[CH2:5][CH2:6][CH2:7][NH:8][CH2:16][CH:17]([OH:18])[CH2:19][OH:20]

Participants

4

Reactant 2

HCID 11164GlycidolHCID 234677983,3'-[(3-Aminopropyl)azanediyl]di(propane-1,2-diol)

Product 1

HCID 23467815N,N,N'-Tri-(2,3-dihydroxypropyl)trimethylenediamine

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

N,N-di-(2,3-dihydroxypropyl)trimethylenediamine (11.1 g., 0.05 mole) was dissolved in 125 ml. of methanol and heated under reflux with agitation. Glycidol (3.7 g., 0.05 mole) was added dropwise over a period of 1.5 hour and the solution mixed an additional hour at 60° C.-80° C. The methyl alcohol and other volatiles were removed by stripping under reduced pressure to leave the product suitable for use in the next steps.

Workup

  1. temperatureunder reflux with agitation
  2. additionthe solution mixed an additional hour at 60° C.-80° C
  3. customThe methyl alcohol and other volatiles were removed
  4. customto leave the product suitable for use in the next steps

Sources & evidence

ORD record
ord-fb4f56bb0b024760b004b9e82e9d52f9
Source dataset
uspto-grants-1977_11
Patent number
US04058625

Reaction notes

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