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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66958Erstellt: 25. Oktober 2026

Sulfuric Acid → 5-Trifluoromethylbenzofuroxan

https://huagongshe.com/reaction/66958

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktUreaHCID 1176—
EduktSodium AzideHCID 33557—
EduktBenzenamine, 2-nitro-4-(trifluoromethyl)-HCID 67865—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt5-TrifluoromethylbenzofuroxanHCID 10262315—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04343942
Quelldatensatzuspto-grants-1982_08
ORD IDord-d3f3645100c54ccf9f2073273a55f333
Quellennotizuspto-grants-1982_08