反应 #3860
ord-d08bf726ee614cf79e621b0c1f4b7772
反应方程式
溶剂
反应条件
后处理
- 1其他was prepared in a 100 ml round bottomed flask
- 2其他equipped with a magnetic stirrer
- 3温度thermometer and reflux condenser
- 4温度The mixture was heated
- 5温度to reflux at 105°-110°
- 6其他were withdrawn periodically
- 7其他partitioned between 1 ml of H2O and 1 ml of hexane
- 8其他at 1.1 and 2.2 and 17 hr
- 9workup.ADDITIONMore potassium carbonate (1.7 g) was added at 212 hr
- 10其他the reaction to completion
- 11温度The reaction mixture was cooled
- 12萃取extracted 3 times with 25 ml of hexane
- 13萃取the organic layer was extracted with water
- 14其他dried
- 15其他the solvent removed
实验过程
(Z,Z)-1,12,14-heptadecatriene (TRIENE) was synthesized conveniently from Wittig Salt and aldehyde in aqueous dioxidepotassium carbonate heterogeneous medium (Lechat 1982). A mixture of 3.57 g (0.01 mol) of methyl triphenylphosphonium bromide (Alfa Inorganics), 1.7 g (0.14 mol) of potassium carbonate, 10 ml of 1,4-dioxane, 0.15 ml of water and 2.36 g (0.01 mol) of (Z,Z)-11,13-hexadecadienal (AL. Albany International) was prepared in a 100 ml round bottomed flask equipped with a magnetic stirrer, thermometer and reflux condenser. The mixture was heated to reflux at 105°-110° with stirring while aliquots of 15 ul were withdrawn periodically and partitioned between 1 ml of H2O and 1 ml of hexane. Analysis by gas-liquid chromatography, showed 66, 70 and 99% triolefin and 30%, 26% and 1% starting aldehyde at 1.1 and 2.2 and 17 hr, respectively. More potassium carbonate (1.7 g) was added at 212 hr to drive the reaction to completion. The reaction mixture was cooled and extracted 3 times with 25 ml of hexane, then the organic layer was extracted with water, dried and the solvent removed to leave 1.8 g of yellow oil and a few crystals of triphenylphosphine oxide. The oil was taken up in hexane and passed through a 1×45 cm column of silica gel (60-200 mesh, Baker) with hexane, to yield 1.7 g (73% yield) of clear oil.