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HRID 1493846作成日:2026年10月26日

Cyproheptadine → [1,1'-Biphenyl]-2,5-dicarboxylic acid, 4'-methyl-, 2,5-dimethyl ester

https://huagongshe.com/reaction/1493846

反応式

関与物質

役割名称HCID仕込み量
反応物CyproheptadineHCID 2913—
反応物4-BromotolueneHCID 7805—
反応物Dimethyl 2-bromoterephthalateHCID 87741—
反応物HCID 178418306HCID 178418306—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418751HCID 178418751—
溶媒TetrahydrofuranHCID 8028—
生成物[1,1'-Biphenyl]-2,5-dicarboxylic acid, 4'-methyl-, 2,5-dimethyl esterHCID 10565585.3%

反応条件

温度0 °C

反応手順

4-Bromotoluene (6 g) was dissolved in tetrahydrofuran (20 ml). To this solution at -78° C. under N2 was added over a ten minute period, 1.7M tBuLi (42 ml). After two hours at room temperature, the reaction mixture was cooled to 0° C. and 1M ZnCl2 (36 ml) was added over a ten minute period. After one half hour at room temperature, bis(triphenylphosphine)nickel(II) chloride (1.32 g) was added followed by dimethyl-2-bromo-terepthalate (6 g) in tetrahydrofuran (20 ml) dropwise over a five minute period. The reactin mixture was stirred at room temperature for two hours. The tetrahydrofuran was removed under reduced pressure. The residue was treated with ethyl acetate and 1N HCl and the layers separated. The organic phase was washed with water, brine, dried over magnesium sulfate and evaporated gave the crude product. Chromatography on silica gel using 5% hexanes/methylene chloride gave the desired product (5.33 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05025007
出典データセットuspto-grants-1991_06
ORD IDord-87573bcf06304a439681c3c29cba30af
出典メモuspto-grants-1991_06