2-Ethylhexanol → Toluene 2,4-Diisocyanate

HRID 328318Notes

Reaction equation

HRID 328318 reaction equation
[CH2:1]([CH:3]([CH2:6][CH2:7][CH2:8][CH3:9])[CH2:4][OH:5])[CH3:2].[CH3:10][C:11]1[CH:16]=[CH:15][C:14]([N:17]=[C:18]=[O:19])=[CH:13][C:12]=1[N:20]=[C:21]=[O:22].C(C(C)=O)CCC>>[NH2:17][C:18]([O:5][CH2:4][CH3:3])=[O:19].[CH2:1]([CH:3]([CH2:6][CH2:7][CH2:8][CH3:9])[CH2:4][OH:5])[CH3:2].[CH3:10][C:11]1[CH:16]=[CH:15][C:14]([N:17]=[C:18]=[O:19])=[CH:13][C:12]=1[N:20]=[C:21]=[O:22]

Participants

5

Reactant 3

HCID 77202-EthylhexanolHCID 11443Toluene 2,4-DiisocyanateHCID 115832-Hexanone

Product 2

HCID 11443Toluene 2,4-DiisocyanateHCID 879616842-Ethylhexanol monourethane

Procedure

A 2-ethylhexanol monourethane of 2,4-toluene diisocyanate was prepared by adding 1953 parts of 2-ethylhexanol to an agitated mixture of 2610 parts of 2,4-TDI and 200 parts of methyl butyl ketone over approximately a 3 hour period with external cooling to maintain the reaction temperature below 18° C. After the addition was completed, the product was stored under dry nitrogen for subsequent use.

Workup

  1. temperaturewith external cooling
  2. temperatureto maintain the reaction temperature below 18° C
  3. additionAfter the addition

Sources & evidence

ORD record
ord-08fa460d5c1442dbaf787e9c7eb534b7
Source dataset
uspto-grants-1977_04
Patent number
US04017438

Reaction notes

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