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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326027생성일: 2026년 10월 24일

Benzene → 4-Bromo-2-fluoro-1,1'-biphenyl

https://huagongshe.com/ko/reaction/326027

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물Isoamyl NitriteHCID 8053—
반응물4-Bromo-2-fluoroanilineHCID 123050—
촉매IronHCID 23925—
촉매ZincHCID 23994—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물4-Bromo-2-fluoro-1,1'-biphenylHCID 521063—

반응 단계

Solutions of 375 ml (325 g, 2.8 moles) of isoamyl nitrite, and of 378 grams (2.0 moles) of crude 4-bromo-2-fluoroaniline in 250 ml benzene are added separately and simultaneously dropwise over about 20 hours to 3500 ml of benzene vigorously stirred under a nitrogen atmosphere, and kept in a water bath at 65° C. The mixture is kept overnight at 65° C., then cooled, washed twice with 250 ml of water and evaporated. The dark oily residue is dissolved in 750 ml methanol and 450 ml concentrated hydrochloric acid, and treated with 138 grams (2.1 moles) of granular zinc, added in small portions over about 6 hours. In order to complete this "reductive upgrading", the solution is treated with 54 grams (1.0 mole) of fine iron filings over 0.5 hours. Within one hour the color of the mixture is visibly lighter. The solution is diluted with one liter of water and one liter of Skellysolve B hexanes, and the liquids are decanted from the remaining metals. The aqueous phase is extracted twice with one liter of Skellysolve B hexanes and the one liter of water, one liter of 1 N NaOH, and one liter of water. The solution is then passed through anhydrous sodium sulfate and evaporated to provide 389 grams of 4-bromo-2-fluoro-biphenyl.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04443631
출처 데이터셋uspto-grants-1984_04
ORD IDord-601a58a21c684548beb39da1256352bc
출처 메모uspto-grants-1984_04