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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2354498생성일: 2026년 10월 26일

Cyclohexane → 1-Pentadecene-5-phosphonic acid diethyl ester

https://huagongshe.com/reaction/2354498

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexaneHCID 8078—
반응물1-IododecaneHCID 16314—
반응물(4-Pentenyl)phosphonic acid diethyl esterHCID 13462469—
반응물CID 53628100HCID 178418400—
용매TetrahydrofuranHCID 8028—
생성물1-Pentadecene-5-phosphonic acid diethyl esterHCID 2105414073%

반응 조건

온도0 °C

반응 단계

A solution of 4-pentenyl phosphonic acid diethyl ester (2.832 g, 13.7 mmol) in anhydrous tetrahydrofuran (20 mL) and cooled to about −78° C. A 1.3 M solution of sec-butyl lithium in cyclohexane (15 mL, 19.5 mmol) was added slowly to the mixture keeping the temperature below −60° C. 1-Iododecane (6.32 g, 23.6 mmol, 1.8 eq.) was then added slowly to the reaction mixture. The mixture was warmed to 0° C. and was stirred for three hours. The reaction was then quenched with NH4Cl (saturated, 20 mL). The mixture was warmed to room temperature and the THF was removed by rotary evaporation. The resulting solution was extracted with ethyl acetate (50 mL). The organic layer was separated and dried over Na2CO3. The solvent was removed and the resulting residue was purified by column chromatography (silica, ethyl acetate/hexane=2/8 then 4/6) to provide the pure product (3.46 g, 73% yield). 1H NMR (CDCl3) δ=5.8 (m, 1H), 5.0 (m, 2H), 4.1 (m, 4H), 2.2 (m, 2H), 1.8-1.2 (m, 27H), 0.9 (t, 3 H). 31P NMR (CDCl3) δ=35.8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07754200B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-5fef42b7870649578ef030edbc0ec62c
출처 메모uspto-grants-2010_07