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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417698Generated: October 26, 2026

Nitric Acid → 1-Chloro-2-fluoro-4-nitro-5-(trifluoromethyl)benzene

https://huagongshe.com/reaction/2417698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantBenzene, 2-chloro-1-fluoro-4-(trifluoromethyl)-HCID 157153—
Product1-Chloro-2-fluoro-4-nitro-5-(trifluoromethyl)benzeneHCID 20163306—

Reaction Conditions

Temperature40 °C

Reaction Steps

About 500 parts of aqueous nitric acid was added slowly, with stirring, to a reaction vessel containing about 400 parts of 3-chloro-4-fluorobenzotrifluoride. The temperature of the reaction mixture was maintained at about 40° C. during the addition, then raised to about 60° C. and maintained thereat for about 5 hours. The reaction mixture was allowed to settle. The aqueous layer was removed and the organic layer was washed twice with 500 parts of water, treated several times with a saturated solution of sodium bicarbonate, washed with water again, dried over anhydrous magnesium sulfate, and filtered. The filtrate was distilled at reduced pressure to yield 347 parts of 5-chloro-4-fluoro-2-nitrobenzotrifluoride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04469893
Source datasetuspto-grants-1984_09
ORD IDord-d5e5dea3eb8046218951f189f2a249a1
Source noteuspto-grants-1984_09