反应 #6068

反应方程式

phenyl vinyl sulfide

dimethyl fumarate

ethylaluminum dichloride

→

title compound

Dimethyl 3-(phenylthio)cyclobutane-1,2-dicarboxylate

溶剂

hexane

1,2-dichloroethane

1,2-dichloroethane

反应条件

后处理

1. 1
   温度The resultant yellow solution was heated
2. 2
   温度to reflux
3. 3
   workup.STIRRINGto stir
4. 4
   温度at reflux for 3 h
5. 5
   其他the reaction was quenched carefully with 100 mL of 1.0 N hydrochloric acid solution
6. 6
   萃取the reaction mixture was extracted with 3×50 mL of ethyl acetate
7. 7
   萃取The organic extract
8. 8
   洗涤was washed with 2×50 mL of water and 50 mL of brine
9. 9
   干燥dried over anhydrous magnesium sulfate
10. 10
    过滤filtered
11. 11
    浓缩concentrated to a viscous orange oil
12. 12
    其他The oil (1.56 g) was chromatographed on silica gel (25 g)
13. 13
    洗涤eluted with 300 mL of 3% ethyl acetate in 1,2-dichloroethane
14. 14
    workup.DISTILLATIONThe resultant yellow oil was purified by bulb-to-bulb distillation

实验过程

To a solution of 1.06 g (7.34 mmol) of dimethyl fumarate in 20 mL of dry 1,2-dichloroethane under nitrogen atmosphere, was added with stirring, 7.34 mmol of a 1.0 M solution of ethylaluminum dichloride in hexane. The resultant yellow solution was heated to reflux and a solution of 1.0 g (7.34 mmol) of phenyl vinyl sulfide in 4 mL of dry 1,2-dichloroethane was added dropwise, via syringe, over a period of 20 minutes. The reaction mixture was allowed to stir at reflux for 3 h. After cooling to ambient temperature, the reaction was quenched carefully with 100 mL of 1.0 N hydrochloric acid solution and the reaction mixture was extracted with 3×50 mL of ethyl acetate. The organic extract was washed with 2×50 mL of water and 50 mL of brine, dried over anhydrous magnesium sulfate, filtered and concentrated to a viscous orange oil. The oil (1.56 g) was chromatographed on silica gel (25 g) eluted with 300 mL of 3% ethyl acetate in 1,2-dichloroethane. The resultant yellow oil was purified by bulb-to-bulb distillation to give the title compound as a yellow oil; b.p 120° C. (0.05 mm Hg); EI-MS, m/e (relative intensity): 280 (M+, 18), 136 (100), 91 (13); 1H NMR (CDCl3) δ2.20 (q, 1H), 2.61 (m, 1H), 3.22 (q, 1H), 3.34 (t, 1H), 3.66 (s, 3H), 3.67 (s, 3H), 3.87 (m, 1H), 7.30 (m, 5H).

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