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

Temperatur

0 °C

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-lododecane (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, 3H). 31P NMR (CDCl3) δ=35.8.

1. customthe temperature below −60° C
2. addition1-lododecane (6.32 g, 23.6 mmol, 1.8 eq.) was then added slowly to the reaction mixture
3. customThe reaction was then quenched with NH4Cl (saturated, 20 mL)
4. temperatureThe mixture was warmed to room temperature
5. customthe THF was removed by rotary evaporation
6. extractionThe resulting solution was extracted with ethyl acetate (50 mL)
7. customThe organic layer was separated
8. dry with materialdried over Na2CO3
9. customThe solvent was removed
10. customthe resulting residue was purified by column chromatography (silica, ethyl acetate/hexane=2/8

ORD-Eintrag

ord-6b024941c52b4a698225ccfdbbb3370d

Quelldatensatz

uspto-grants-2006_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07109184B2