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HRID 2227698作成日:2026年10月26日

Toluene → HCID 18504279、化合物

https://huagongshe.com/reaction/2227698

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Sodium CarbonateHCID 10340—
反応物Diphenyl-(4-(4,4,5,5-tetramethyl-(1,3,2)dioxaborolan-2-yl)-phenyl)-amineHCID 11639307—
反応物2-Bromo-1,4-bis(acetyloxymethyl)benzeneHCID 18504280—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒WaterHCID 962—
生成物HCID 18504279HCID 1850427975.2%

反応手順

4-Diphenylamino-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene (6.09 g) was prepared by adding butyllithium (0.64 g dissolved in 4 mL hexane) was added into a solution of 4-bromotriphenylamine (3.24 g) in 50 mL tetrahydrofuran at −78° C. The mixture was stirred while the solution temperature warmed up to 10° C. It was cooled again to −78° C. when borolane (2.23 g) was added. The mixture was then stirred at room temperature for 20 hrs and poured into water. The product was extracted with ether, washed with brine, and dried with MgSO4. Solvent was evaporated. The residue was chromatographed on a silica gel column using a hexane/ethyl acetate mixture as eluent (40:1). 2.03 g of the product, 4-diphenylamino-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, was obtained. Then, 4-diphenylamino-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene (6.09 g), 2-bromo-1,4-bis(acetyloxymethyl)benzene (4.9 g), tetrakis(triphenylphosphine)-palladium(0) (0.15 g), toluene (15 mL), and an aqueous solution of sodium carbonate (2M, 25 mL) were mixed under argon. The resulting mixture was stirred at reflux for 2 days, cooled, and poured into water. The aqueous mixture was then extracted with ether. The etheral solution was washed with dilute HCl, brine, dried with magnesium sulfate, and evaporated. The residue was recrystallized in methanol to yield 5.70 g of 2-(4-diphenylamino-phenyl)-1,4-bis(acetyloxymethyl)benzene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06414104B1
出典データセットuspto-grants-2002_07
ORD IDord-6d7377c3f58e47d9a31ee1f16c665f37
出典メモuspto-grants-2002_07