HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652058Generated: November 3, 2026
Hydrochloric Acid → 4-(5-Trifluoromethylpyrid-2-yloxy)phenylisocyanate
https://huagongshe.com/reaction/652058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 4-{[5-(Trifluoromethyl)pyridin-2-yl]oxy}aniline | HCID 2783085 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 4-(5-Trifluoromethylpyrid-2-yloxy)phenylisocyanate | HCID 14053350 | 90% |
Reaction Steps
20.3 g (0.08 mol) of 4-(5-trifluoromethylpyrid-2-yloxy)aniline are dissolved in 200 ml of dry chlorobenzene. This solution is cooled to -20° C. and rapidly added a solution of 3.7 g of gaseous HCl in 80 ml of dry chlorobenzene. The resultant crystalline slurry is cooled to -30° C. and a strong flow of about 40 g of phosgene is introduced over 1 hour. The addition of phosgene is then discontinued and the reaction mixture is stirred for 1 hour at 20° C. and subsequently for 1 hour in an oil bath at 110° C. A clear solution forms which is then cooled in a stream of nitrogen and, with stirring, excess phosgene is expelled with nitrogen. First the chlorobenzene is distilled off under normal pressure and then the isocyanate is distilled off under a high vaccum. Boiling point 105°-107° C./0.03 mbar; yield>90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04670441 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-d050fb09f5834925a1fa75e709fa8711 |
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| Source note | uspto-grants-1987_06 |
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