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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 399346생성일: 2026년 10월 26일

Bis(eta-cyclopentadienyl) iron → 1,1'-Bis[2,4,8,10-tetrakis(tert-butyl)-dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl]ferrocene

https://huagongshe.com/reaction/399346

반응식

참여 물질

역할이름HCID투입량
반응물Bis(eta-cyclopentadienyl) ironHCID 7611—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물2,4,8,10-Tetra-tert-butyl-6-chlorodibenzo[d,f][1,3,2]dioxaphosphepineHCID 10983610—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물1,1'-Bis[2,4,8,10-tetrakis(tert-butyl)-dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl]ferroceneHCID 13172087547%

반응 단계

To a solution of 9.5 g (50 mmol) of ferrocene in 250 mL of hexane is added dropwise 67 mL of a 1.6M solution of n-butyl lithium at ambient temperature. The reaction mixture is stirred for 20 minutes and then to the resultant red suspension is added 12.0 g (103 mmol) of N,N,N',N'-tetramethylethylenediamine. A slight exotherm of 10° C. is observed. The reaction mixture is then heated at reflux for two hours during which time an orange suspension forms. The reaction mixture is cooled to room temperature and 100 mL of tetrahydrofuran is then added. The reaction mixture is cooled to -40° C. Then to the cooled reaction mixture is added dropwise a solution of 51.8 g (109 mmol) of 2,4,8,10-tetrakis(tert-butyl)-6-chloro-dibenzo[d,f][1,3,2]dioxaphosphepin in 100 mL of tetrahydrofuran. The reaction mixture is allowed to warm to ambient temperature after the addition is complete. The reaction mixture is then heated at reflux for six hours. After cooling, the mixture is filtered and the filtrate is concentrated under reduced pressure. The residue formed is triturate with 150 mL of hexane. The resultant solid is recrystallized from acetonitrile/tetrahydrofuran mixture to give 25 g (47% yield) of a light brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05817850
출처 데이터셋uspto-grants-1998_10
ORD IDord-f1bed6f8468948ecad9265df06b35205
출처 메모uspto-grants-1998_10