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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476322생성일: 2026년 10월 24일

1,2-Bis(dichlorophosphino)benzene → 1,2-Bis(bis(4-fluorophenyl)phosphino)benzene

https://huagongshe.com/ko/reaction/476322

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Bis(dichlorophosphino)benzeneHCID 3316562—
반응물HCID 178418676HCID 178418676—
용매TetrahydrofuranHCID 8028—
생성물1,2-Bis(bis(4-fluorophenyl)phosphino)benzeneHCID 5293791262%

반응 단계

A THF solution (26.6 mL, 1.03 M, 27.40 mmol) of p-fluorophenylmagnesium bromide was added to a mixture of 1,2-bis(dichlorophosphino)benzene (0.96 g, 3.43 mmol) and THF (20 mL) in an argon atmosphere at −78° C. After warming to room temperature, the mixture was allowed to react overnight at 60° C. The reaction mixture was cooled to ambient temperature, and the solvent was removed under reduced pressure; subsequently, CH2Cl2 (30 mL) was added. 1N aqueous solution of hydrochloric acid (20 mL) was added to the reaction mixture, and the aqueous layer was extracted three times with CH2Cl2. The moisture contained in the combined organic extract was removed with magnesium sulfate, and the extract was filtered. After removing the solvent under reduced pressure, the resulting yellow oily substance was triturated with methanol to give a white powder, and the white powder was washed two times with methanol, giving the title compound as a white powder (1.10 g, yield 62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637710B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-e2887f65a4a64def8574959fa4dd001b
출처 메모uspto-grants-2014_01