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HRID 276071作成日:2026年10月26日

Iodobenzene → 3-Fluoro-4-methylbiphenyl

https://huagongshe.com/reaction/276071

反応式

関与物質

役割名称HCID仕込み量
反応物IodobenzeneHCID 11575—
反応物4-Bromo-2-fluorotolueneHCID 171040—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物3-Fluoro-4-methylbiphenylHCID 1612750299.1%

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06352985B1
出典データセットuspto-grants-2002_03
ORD IDord-58153a43c1514d19abfc18e4b3526ee6
出典メモuspto-grants-2002_03