참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclohexane | HCID 8078 | — |
| 반응물 | 1-Iododecane | HCID 16314 | — |
| 반응물 | (4-Pentenyl)phosphonic acid diethyl ester | HCID 13462469 | — |
| 반응물 | CID 53628100 | HCID 178418400 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Pentadecene-5-phosphonic acid diethyl ester | HCID 21054140 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07754200B2 |
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| 출처 데이터셋 | uspto-grants-2010_07 |
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| ORD ID | ord-5fef42b7870649578ef030edbc0ec62c |
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| 출처 메모 | uspto-grants-2010_07 |
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