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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1493846생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1493846

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참여 물질

역할이름HCID투입량
반응물CyproheptadineHCID 2913—
반응물4-BromotolueneHCID 7805—
반응물Dimethyl 2-bromoterephthalateHCID 87741—
반응물HCID 178418306HCID 178418306—
촉매ZincchlorideHCID 3007855—
촉매HCID 178418751HCID 178418751—
용매TetrahydrofuranHCID 8028—
생성물[1,1'-Biphenyl]-2,5-dicarboxylic acid, 4'-methyl-, 2,5-dimethyl esterHCID 10565585.3%

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05025007
출처 데이터셋uspto-grants-1991_06
ORD IDord-87573bcf06304a439681c3c29cba30af
출처 메모uspto-grants-1991_06