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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54912생성일: 2026년 10월 24일

Water → Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate

https://huagongshe.com/ko/reaction/54912

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Tetraisopropyl methylenediphosphonateHCID 74266—
반응물(2E,6E)-1-bromo-3,7,11-trimethyldodeca-2,6,10-trieneHCID 5366048—
용매1,2-DimethoxyethaneHCID 8071—
생성물Tetraisopropyl (E,E)-farnesylmethylenebisphosphonateHCID 8675076060.9%

반응 단계

Oily sodium hydride (60%, 0.24 g) was added to a solution of tetraisopropyl methylenebisphosphonate (3.44 g) in dimethoxyethane (25 ml). The mixture was stirred at room temperature for 1 hour. Then, a solution of (E,E)-farnesyl bromide (1.43 g) in dimethoxyethane (5 ml) was added dropwise at 0° C. The reaction mixture was stirred at room temperature for 1 hour, then poured into water and extracted with ethyl acetate. The organic layer was washed with water and dried (MgSO4), and then the solvent was distilled off under reduced pressure. The oily residue was subjected to column chromatography on silica gel. Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate (1.67 g, 60.9%) was obtained as an oil from the fractions obtained by elution with ethyl acetate-chloroform (1:1, v/v).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624917
출처 데이터셋uspto-grants-1997_04
ORD IDord-73a7b1d009aa461cb31c197a6b725fa7
출처 메모uspto-grants-1997_04