Ethanolamine → HCID 86739068, compound

HRID 1463104Notes

Reaction equation

HRID 1463104 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, was added over a 5-10 minute period to half-blocked isophorone diisocyanate, 65.8 g, prepared according to Example I. During addition of the ethanolamine, the reaction mixture was maintained at a temperature of 90° C. After addition was completed, the reaction mixture was stirred for 3 hours, was then diluted with the glycol ether ester solvent Ektasolve E.P. (trademark, Eastman Kodak Company, Rochester, N.Y.), 20 g, and was then stored. The product oligomer was characterized by its infrared spectrum which showed a absence of the 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. customa absence of the absorption at 2250 cm-1

Sources & evidence

ORD record
ord-2efdd7c36521435981d7192b37450935
Source dataset
uspto-grants-1984_07
Patent number
US04463143

Reaction notes

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