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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66958생성일: 2026년 10월 26일

Sulfuric Acid → 5-Trifluoromethylbenzofuroxan

https://huagongshe.com/reaction/66958

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물UreaHCID 1176—
반응물Sodium AzideHCID 33557—
반응물Benzenamine, 2-nitro-4-(trifluoromethyl)-HCID 67865—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물5-TrifluoromethylbenzofuroxanHCID 10262315—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04343942
출처 데이터셋uspto-grants-1982_08
ORD IDord-d3f3645100c54ccf9f2073273a55f333
출처 메모uspto-grants-1982_08