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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128064생성일: 2026년 10월 25일

Chlorodiphenylphosphine → Diphenylphosphine

https://huagongshe.com/reaction/128064

반응식

참여 물질

역할이름HCID투입량
반응물ChlorodiphenylphosphineHCID 66180—
반응물LithiumHCID 3028194—
용매TetrahydrofuranHCID 8028—
생성물DiphenylphosphineHCID 70017—

반응 단계

A THF solution (150 ml) containing chlorodiphenylphosphine (60 g, 0.34 mole) was added dropwise from a dropping flask, and under nitrogen atmosphere to a stirred THF (75 ml) suspension of lithium metal (5 g, 0.7 moles) in a 500 ml round bottom flask. Formation of lithiodiphenylphosphide was indicated by the appearance of a bright red color. After stirring 18 hours, unreacted lithium was removed and the solution was added slowly to a rapidly stirred THF slurry of the brominated resin beads (32 g, 35 percent Br, 131.3 mmol Br). This slurry was allowed to stir two days under nitrogen (longer if high percent Br content resin used). The slurry was then hydrolyzed by adding it to two liters of nitrogen-saturated acetone/water (3:1) and stirring for one hour. The beads were then filtered and washed by stirring successively in one liter each of the following nitrogen-saturated solvents: water (2 hours), acetone (2 hours), benzene/methanol (9:1) (18-24 hours), and methanol (4-5 hours). The beads were then vacuum dried (80° C., 0.05 torr) for 24 hours, and analyzed for 6.44 percent P which corresponds to 35.0 percent of the polystyryl rings substituted with the diphenylphosphide moiety.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04258206
출처 데이터셋uspto-grants-1981_03
ORD IDord-74a4e650899e4eea8e3cf265b74afb8c
출처 메모uspto-grants-1981_03