Synthetic method of cinnamic acid n-pentyl formate and application of cinnamic acid n-pentyl formate in essence
A technology of n-amyl cinnamate and a synthesis method, which is applied in the preparation of carboxylate, essential oils/fragrance, chemical instruments and methods, etc., can solve the influence of the quantity of varieties and product quality, the inability to meet the demand, the high price, etc. problem, to achieve the effect of small temperature gradient, uniform heating and high selectivity
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Embodiment 1
[0014] A kind of synthetic method of n-pentyl cinnamate, this synthetic route is divided into two steps, the first step solid superacid Ga2O3 / SO4 2- / ZrO2 synthesis, the second step is the synthesis of n-pentyl cinnamate. Using cinnamic acid and n-amyl alcohol as raw materials, according to a certain proportion of substances, adding a catalyst and reacting for a certain period of time under microwave conditions, the target product can be obtained.
[0015] The synthesis of the first step solid super acid is as follows:
[0016] Drop 0.5 mol / L Zr(NO3)4 solution into a vigorously stirred 5 mol / L ammonia solution, adjust the pH value of the suspension to 9-10 with ammonia water, then reflux at 100°C for 24 hours, and filter to obtain Precipitate, then wash and filter repeatedly with deionized water until the pH value is 7.0. Add the 30% Ga2(SO4)3 aqueous solution to the Zr(OH)4 precipitate in a certain proportion, stir for 10 hours, and then dry it at 120°C. Finally, it was ro...
Embodiment 2
[0019] A kind of synthetic method of n-pentyl cinnamate, this synthetic route is divided into two steps, the first step solid superacid Ga2O3 / SO4 2- / ZrO2 synthesis, the second step is the synthesis of n-amyl cinnamate. Using cinnamic acid and n-amyl alcohol as raw materials, according to a certain proportion of substances, adding a catalyst and reacting for a certain period of time under microwave conditions, the target product can be obtained.
[0020] The synthesis of the first step solid super acid is as follows:
[0021] Drop 0.5 mol / L Zr(NO3)4 solution into a vigorously stirred 5 mol / L ammonia solution, adjust the pH value of the suspension to 9-10 with ammonia water, then reflux at 100°C for 24 hours, and filter to obtain Precipitate, then wash and filter repeatedly with deionized water until the pH value is 7.0. Add the 30% Ga2(SO4)3 aqueous solution to the Zr(OH)4 precipitate in a certain proportion, stir for 10 hours, and then dry it at 120°C. Finally, it was roast...
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