Method for synthesizing veratric acid
A synthesis method and technology of veratrol are applied in chemical instruments and methods, preparation of carboxylate, preparation of organic compounds, etc., can solve the problems of consumption of potassium tert-butoxide, high price of veratrol, etc., and achieve a short production cycle. , the effect of reducing costs and reducing environmental pollution
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Embodiment 1
[0018] (1) Preparation of Veratrate:
[0019] In the flask equipped with stirring, condenser and thermometer, add veratraldehyde (33.2g, 0.20mol), calcium hydroxide (74g, 1.0mol), isopropanol aqueous solution (250mL, water content is 10% (v) ), formalin solution (45.0g, 35%wt), and reacted for 2.5h at a temperature of about 50°C. Filtration yielded a yellow solid, veratrate.
[0020] (2) Preparation of veratrol product:
[0021] At room temperature, sulfuric acid aqueous solution (20%wt) was added dropwise to veratrate for 0.5h, and the pH at the end point of acidification was 4. After filtering, washing and drying, 16.32 g of a light yellow solid was obtained, which was a veratronic acid product, and the yield was 88.5%.
[0022] The measurement results of the physical properties of the veralic acid product: a light yellow solid with a melting point of 177-178°C, which is consistent with the value in the literature (Phytochemistry, 1990, 29(3), 1014-1016).
[0023] Gas ch...
Embodiment 2
[0026] In the flask equipped with stirring, condenser and thermometer, add veratraldehyde (63.1g, 0.38mol), sodium carbonate (60.4g, 0.57mol), n-butanol aqueous solution (550mL, water content is 15% (v) ), formalin solution (60.0g, 35%wt), and reacted for 1.5h at a temperature of about 50°C. A yellow solid was obtained as veratrate. At room temperature, sulfuric acid aqueous solution (30%wt) was added dropwise to the veratrate for 2 hours, and the pH at the end point of the acidification was 2. 28.95 g of the product was obtained, and the yield was 82.6%.
Embodiment 3
[0028] In the flask equipped with stirring, condenser and thermometer, add veratraldehyde (107.9g, 0.65mol), potassium hydroxide (218.4g, 3.9mol), aqueous ethanol (700mL, water content is 25% (v)) , Paraformaldehyde (97.5g, 3.25mol), reacted at a temperature of about 100°C for 4h. A yellow solid was obtained as veratrate. At room temperature, nitric acid aqueous solution (5%wt) was added dropwise to veratrate for 1.5h, and the pH at the end point of acidification was 3. 56.16 g of the product was obtained with a yield of 93.7%.
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