HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 1,3-Dichloro-5-isocyanato-2-(1,1,2,2-tetrafluoroethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2,6-Dichloro-4-amino-(1,1,2,2-tetrafluoroethoxy)benzene | HCID 5463763 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 1,3-Dichloro-5-isocyanato-2-(1,1,2,2-tetrafluoroethoxy)benzene | HCID 20230152 | — |
Reaction Steps
33.4 g of 3,5-dichloro-4-(1,1,2,2,-tetrafluoroethoxy)aniline are dissolved in 130 ml of chlorobenzene. With stirring, this solution is added dropwise at 22° C. to a solution consisting of 90 g of toluene containing 20% by weight of phosgene and of 100 ml of dioxane and 300 ml of chlorobenzene. The reaction mixture is stirred for 1 hour at room temperature, 1 hour at 50° C. and then 1 hour at 80° C. The reaction mixture is subsequently concentrated in a water-jet vacuum and then distilled under high vacuum, affording the title compound of the formula ##STR8## as a colourless oil. Boiling point 81°-83° C./2.5 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04618608 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-fb294e807b9940a6a7d32f33580ea77c |
| Source note | uspto-grants-1986_10 |