Réaction #1552020

ord-2b6f222daf9d48228cd998c5893a0e94

Équation de réaction

Clc1ccccc1Cl
ortho dichlorobenzene
O=C(Cl)Cl
phosgene
O
water
O=C(Cl)Cl
phosgene
O=C(Cl)Cl
phosgene
NCC1CCC(CN)CC1
1,4-bis(aminomethyl)cyclohexane
Clc1ccccc1Cl
ortho dichlorobenzene
NCC1CCC(CN)CC1
1,4-bis(aminomethyl)cyclohexane
O=C=NCC1CCC(CN=C=O)CC1
1,4-bis(isocyanatomethyl)cyclohexane
Rendement 90.0%

Conditions de réaction

Température
150°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreSpecifically, a stirring rod, a thermometer, a phosgene inlet tube, a dropping funnel, and a condenser tube were attached to a flask
  2. 2
    Autrewas lowered to 10° C. or below
  3. 3
    workup.ADDITIONthe mixed solution was added into the flask over 30 minutes
  4. 4
    TempératureDuring this time, the temperature in the flask was maintained at 30° C. or below
  5. 5
    workup.ADDITIONAfter completion of the addition
  6. 6
    Autrea white slurry-like liquid was formed in the flask
  7. 7
    AutreAfter completion of the reaction, nitrogen gas
  8. 8
    workup.ADDITIONwas introduced at a temperature of 100 to 150° C. at a flow rate of 10 L/hour
  9. 9
    Autrefor degassing
  10. 10
    workup.DISTILLATIONThe ortho dichlorobenzene solvent was distilled away under reduced pressure
  11. 11
    workup.ALIQUOTwas further sampled by vacuum distillation

Mode opératoire

As a raw material, 1,4-bis(aminomethyl)cyclohexane (manufactured by Mitsubishi Gas Chemical Company, Inc.) having a trans-isomer/cis-isomer ratio of 93/7 determined by 13C-NMR was used to perform cold/hot two-stage phosgenation method under normal pressure. Specifically, a stirring rod, a thermometer, a phosgene inlet tube, a dropping funnel, and a condenser tube were attached to a flask, and the flask was charged with 400 parts by mass of ortho dichlorobenzene. While the flask was cooled with cold water, the temperature in the flask was lowered to 10° C. or below, and 280 parts by mass of phosgene was introduced thereinto from the phosgene inlet tube. The dropping funnel was charged with a mixed solution of 100 parts by mass of 1,4-bis(aminomethyl)cyclohexane and 500 parts by mass of ortho dichlorobenzene, and the mixed solution was added into the flask over 30 minutes. During this time, the temperature in the flask was maintained at 30° C. or below. After completion of the addition, a white slurry-like liquid was formed in the flask. Again, the reaction temperature was increased to 150° C. while introducing phosgene, and the reaction was continued at 150° C. for 5 hours. The reaction solution in the flask became a pale-brown transparent liquid. After completion of the reaction, nitrogen gas was introduced at a temperature of 100 to 150° C. at a flow rate of 10 L/hour for degassing. The ortho dichlorobenzene solvent was distilled away under reduced pressure and a fraction having a boiling point of 138 to 140° C./0.7 KPa was further sampled by vacuum distillation. Thus, 123 parts by mass (90% yield) of 1,4-bis(isocyanatomethyl)cyclohexane was obtained in the form of a colorless and transparent liquid. The resulting 1,4-bis(isocyanatomethyl)cyclohexane had a purity, which was determined by gas chromatography, of 99.9%, a hue of 5 in APHA, and a trans-isomer/cis-isomer ratio, which was determined by 13C-NMR, of 93/7. Hereinafter, 1,4-bis(isocyanatomethyl)cyclohexane having a trans-isomer/cis-isomer ratio of 93/7 is referred to as “BIC93”.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08998749B2uspto-grants-2015_04