Ethanolamine → HCID 86739068, compound

HRID 1463105Notes

Reaction equation

HRID 1463105 reaction equation
[CH2:1]([CH2:3][NH2:4])[OH:2].[O:5]=[C:6]=[N:7]C1CC(C)(C)CC(C)(C[N:12]=[C:13]=[O:14])C1>>[NH2:7][C:6]([O:2][CH2:1][CH3:3])=[O:5].[NH2:12][C:13]([NH2:4])=[O:14].[N-:7]=[C:6]=[O:5].[N-:7]=[C:6]=[O:5]

Participants

3

Reactant 2

HCID 700Ethanolamine2×HCID 169132Isophorone diisocyanate

Product 1

HCID 86739068HCID 86739068, compound

Conditions

Temperature
90 °C

Procedure

Ethanolamine, 6.1 g, is added over a 5-10 minute period to half-blocked isophorone diisocyanate, 53.3 g, prepared according to the method of Example VII. During addition of the ethanolamine, the reaction mixture is maintained at a temperature of 90° C. After addition is completed, the reaction mixture is stirred for 3 hours, diluted with the glycol ether ester solvent Ektasolve E.P. (trademark, Eastman Kodak Company, Rochester, N.Y.) 20. g, and then stored. The product oligomer is characterized by its infrared spectrum which shows the absence of the isocyanate absorption at 2250 cm-1, and the presence of urethane and urea carbonyl absorptions in the 1670-1710 cm-1 region.

Workup

  1. customprepared
  2. additionAfter addition
  3. customthe absence of the isocyanate absorption at 2250 cm-1

Sources & evidence

ORD record
ord-adbfa2363b3c422fbb6f2fac4c0579d0
Source dataset
uspto-grants-1984_07
Patent number
US04463143

Reaction notes

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