Phosgene → 2,5-Bis(2,2,2-trifluoroethoxy)phenyl isocyanate

HRID 1834782Notes

Reaction equation

HRID 1834782 reaction equation
[C:1](Cl)(Cl)=[O:2].[F:5][C:6]([F:23])([F:22])[CH2:7][O:8][C:9]1[CH:15]=[CH:14][C:13]([O:16][CH2:17][C:18]([F:21])([F:20])[F:19])=[CH:12][C:10]=1[NH2:11]>C1(C)C=CC=CC=1>[F:5][C:6]([F:22])([F:23])[CH2:7][O:8][C:9]1[CH:15]=[CH:14][C:13]([O:16][CH2:17][C:18]([F:21])([F:19])[F:20])=[CH:12][C:10]=1[N:11]=[C:1]=[O:2]

Participants

4

Procedure

To a cooled (15°-20° C.) solution of 67.6 g. (0.684 mole) of phosgene in 250 ml. of toluene is added dropwise over one hour a solution of 49.5 g. (0.171 mole) of 2,5-bis-(2,2,2-trifluoroethoxy)aniline in 350 ml. of toluene. After addition is complete, stirring is continued for 30 minutes, then the mixture is heated to its reflux temperature and maintained at reflux for 30 minutes. The solution is evaporated to provide a liquid residue which gradually crystallizes. The solid is recrystallized from heptane to provide 2,5-bis(2,2,2-trifluoroethoxy)phenyl isocyanate as a white solid, m.p. 50°-52° C.

Workup

  1. temperatureTo a cooled (15°-20° C.) solution of 67.6 g
  2. additionAfter addition
  3. temperaturethe mixture is heated to its
  4. temperaturereflux temperature
  5. temperaturemaintained
  6. temperatureat reflux for 30 minutes
  7. customThe solution is evaporated
  8. customto provide a liquid residue which
  9. customgradually crystallizes
  10. customThe solid is recrystallized from heptane

Sources & evidence

ORD record
ord-5f58dd70e3ba44e080e7a704c696beaa
Source dataset
uspto-grants-1978_01
Patent number
US04071524

Reaction notes

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