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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834034Generated: November 1, 2026

Sulfuric Acid → 4-Fluoro-3-(trifluoromethyl)phenol

https://huagongshe.com/reaction/1834034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant4-Fluoro-3-(trifluoromethyl)anilineHCID 75377—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product4-Fluoro-3-(trifluoromethyl)phenolHCID 60185452%

Reaction Conditions

Temperature65 °C

Reaction Steps

70 g (0.39 mol) of 4-fluoro-3-trifluoromethylaniline, prepared according to G.C. Finger and colleagues, Journal of Med. Chem., 7, (1964), 572, are added a little at a time, while stirring, to 500 ml of a 2.5 N solution of sulphuric acid heated to a temperature of 65° C. The solution obtained is cooled to 0° C and 27 g of sodium nitrite dissolved in 45 ml of water are added whilst continuing the stirring and ensuring that the temperature does not exceed +5° C. After the end of the addition, the mixture is stirred for a further hour, during which it becomes perfectly clear. Thereafter, whilst carrying out a steam distillation, the cold solution of the diazonium salt is introduced dropwise into a mixture of 56g of copper sulphate, 21 g of urea, 70 ml of water and 2 ml of concentrated sulphuric acid. The speed of addition is regulated so that the phenol formed is immediately carried away. The distillate is cooled and is extracted repeatedly with ether. The ether solutions are combined and dried, the solvent is driven off and the residue is rectified. 37 g (yield: 52%) of 4-fluoro-3-trifluoromethyl-phenol, distilling at 84° C under 15 mm, are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04067996
Source datasetuspto-grants-1978_01
ORD IDord-6d9ba2edb46645a783bd249e5293bc9d
Source noteuspto-grants-1978_01