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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276071생성일: 2026년 10월 25일

Iodobenzene → 3-Fluoro-4-methylbiphenyl

https://huagongshe.com/reaction/276071

반응식

참여 물질

역할이름HCID투입량
반응물IodobenzeneHCID 11575—
반응물4-Bromo-2-fluorotolueneHCID 171040—
촉매ZincchlorideHCID 3007855—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물3-Fluoro-4-methylbiphenylHCID 1612750299.1%

반응 조건

온도-78 °C

반응 단계

Thirty milliliters of a 1.6-M-n-butyllithium hexane solution and a solution of 9.21 g of 4-bromo-2-fluorotoluene in 30 ml of tetrahydrofuran were added in this order to 30 ml of tetrahydrofuran which had been cooled to −78° C. in a nitrogen atmosphere, and the mixture was then stirred at −78° C. for 1 hour. A solution containing 6.64 g of zinc chloride which had been dehydrated through heat-melting under reduced pressure in 30 ml of tetrahydrofuran was added thereto at −78° C., and the mixture was stirred at room temperature for 1 hour. The reaction solution was added to a solution of 6.63 g of iodobenzene and 0.52 g of tetrakis(triphenylphosphine)palladium (0) in 30 ml of tetrahydrofuran at room temperature, and the mixed solution was stirred for 24 hours. The reaction solution was diluted with 300 ml of ethyl acetate, and the dilute solution was extracted with the addition of 10% hydrochloric acid. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried, and then concentrated. The residue was purified through silica-gel column chromatography (eluent: hexane) to give 6.00 g of oily 3-fluoro-4-methylbiphenyl.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352985B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-58153a43c1514d19abfc18e4b3526ee6
출처 메모uspto-grants-2002_03