HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979627Generated: October 26, 2026
3-(Trifluoromethyl)phenyl isocyanate → 3-(Trifluoromethyl)phenyl carbamic fluoride
https://huagongshe.com/reaction/1979627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)phenyl isocyanate | HCID 9483 | — |
| Reactant | Carbonyl fluoride | HCID 9623 | — |
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | HCID 178506046 | HCID 178506046 | — |
| Product | 3-(Trifluoromethyl)phenyl carbamic fluoride | HCID 20439613 | — |
Reaction Steps
3-(Trifluoromethyl)phenyl carbamic fluoride was prepared in situ by the reaction of 187 parts of 1-isocyanato-3-(trifluoromethyl)benzene and 370 parts of hydrogen fluoride added over a period of about 15 minutes at about 4° C. The reaction mixture was then sealed in a polytetrafluoroethylene reaction vessel, heated to about 24° C., and maintained thereat, with agitation, for about 96 hours. The reaction vessel was then opened to atmospheric pressure and most of the hydrogen fluoride and carbonyl fluoride gases removed. The remaining organic product was analyzed by gas chromatographic techniques, using n-pentadecane as an internal standard, indicating a yield of 41 parts of 3-(trifluoromethyl)benzenamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04481370 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-5d60a0c9f7294859ab4becaba6436242 |
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| Source note | uspto-grants-1984_11 |
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