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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
ReactantCarbonyl fluorideHCID 9623—
ReactantHydrofluoric AcidHCID 14917—
ReactantHCID 178506046HCID 178506046—
Product3-(Trifluoromethyl)phenyl carbamic fluorideHCID 20439613—

Reaction Conditions

Temperature24 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04481370
Source datasetuspto-grants-1984_11
ORD IDord-5d60a0c9f7294859ab4becaba6436242
Source noteuspto-grants-1984_11