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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607723Generated: November 1, 2026

Sulfuric Acid → 5-Trifluoromethylbenzofuroxan

https://huagongshe.com/reaction/1607723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantUreaHCID 1176—
ReactantSodium AzideHCID 33557—
ReactantBenzenamine, 2-nitro-4-(trifluoromethyl)-HCID 67865—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-TrifluoromethylbenzofuroxanHCID 10262315—

Reaction Steps

A solution of 103 grams (0.5 mole) of 4-amino-3-nitro-benzotrifluoride, 750 ml. of acetic acid and 385 ml. of concentrated sulfuric acid is cooled in an ice-bath with sufficient stirring. Sodium nitrite (38 grams, 0.55 moles) is added portionwise at such a rate that the reaction temperature does not exceed 5° C. After addition is complete, 38 grams of urea is added, and with vigoroug stirring 32.5 grams of sodium azide is then added. Stirring is continued for 20 minutes, then the reaction mixture is poured into 4 liters of ice and water. The crude product, 4-azido-3-nitrobenzotrifluoride is extracted from the aqueous mixture with chloroform. The extract is dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to furnish an oily-residue which is taken up in 800 ml. of toluene. The toluene solution is heated under reflux for 18 hours behind a shatter-proof shield. After cooling to room temperature, the solvent is evaporated and the residue is distilled under reduced pressure. The fraction boiling at 105°-108° C. (16 ml.) is considered to be sufficiently pure 5-trifluoromethylbenzofuroxan; yield, 62.3 (60 percent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866175
Source datasetuspto-grants-1989_09
ORD IDord-f9ddbfc97ea940de9f2ffabd25336dce
Source noteuspto-grants-1989_09