A kind of 3-alkoxy-1,1-dialkylthiopropene derivative and its synthesis method
A technology of dialkylthiopropene and synthesis method, which is applied in the direction of organic chemistry, can solve the problems of low atom utilization rate, less olefins, and narrow application range of substrates, so as to avoid pre-functionalization, simplify synthesis steps, and improve the scope of application. wide effect
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Embodiment 1
[0028]
[0029] The specific process is: weigh dithioketene 2a (111.2 mg, 0.5 mmol), FeCl 3 (4.1mg, 0.025mmol), DABCO·6H 2 O (11.0mg, 0.05mmol) was added to a 25mL sealed tube with a branch, 1,4-Dioxane (3mL) and DTBP (219.2mg, 1.5mmol) were added under a nitrogen atmosphere, and placed in a 130°C oil bath React in 24h. After the reaction is complete, cool to room temperature, filter with diatomaceous earth, and rotary evaporate under reduced pressure to remove the solvent, then column chromatography (petroleum ether (60-90°C) / ethyl acetate: 8:1, v / v) to obtain a light yellow Solid product 1a (122.5 mg, yield 80%). The target product was confirmed by NMR and high-resolution mass spectrometry.
Embodiment 2
[0031]
[0032] The reaction steps and operations are the same as in Example 1, except that the dithioketene added to the reaction system is 2b (150.0 mg, 0.5 mmol). The reaction was stopped, and the target product 1b (146.0 mg, yield 76%) was obtained as a light yellow solid after post-processing. The target product was confirmed by NMR and high-resolution mass spectrometry.
Embodiment 3
[0034]
[0035] The reaction steps and operations are the same as those in Example 1, except that the dithioketene added to the reaction system is 2c (118.0 mg, 0.5 mmol). The reaction was stopped, and the target product 1c (128.0 mg, yield 79%) was obtained as a light yellow solid after post-processing. The target product was confirmed by NMR and high-resolution mass spectrometry.
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