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ChemicalBook CAS DataBase List 2,5-Dimethoxycinnamic acid

2,5-Dimethoxycinnamic acid synthesis

6synthesis methods
Synthesis of 2,5-dimethoxycinnamic acid: 2,5-dimethoxybenzaldehyde, malonic acid and pyridine were added to 100ml three necks, piperidine was added at 90°C, refluxed for 2h, cooled to room temperature, and added 3mol/L hydrochloric acid, resulting in a large amount of white precipitate, suction filtration, the filter cake is washed with water, reconstituted with ethanol, after drying, 2,5-dimethoxycinnamic acid was obtained as pale yellow needle crystals.
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Yield: 51%

Reaction Conditions:

with dipotassium peroxodisulfate;palladium diacetate in 1,4-dioxane;acetic acid at 80; for 24 h;Fujiwara Arylation Carboxylation;

Steps:

General procedure for the synthesis of compounds
General procedure: Typical coupling procedure: Pd(OAc)2 (22 mg, 5 mol%), K2S2O8 (0.81 g 3 mmol), alkene (2 mmol), arene (15 mmol, 7.5 equiv.), acetic acid (8 mL) and cosolvent (2 mL) were placed in a 20 mL scintillation vial containing a magnetic stirrer bar. The flask was sealed with a Teflon-lined crimped cap, and the reaction solution was stirred vigorously at 80 °C 24 h (unless otherwise specified). The reaction solution was cooled to room temperature, CH2Cl2 added, filtered and the solvent removed in vacuo. The residue was purified by column chromatography on silica gel using cyclohexane/ethyl acetate to afford the desired product.

References:

Jones, Roderick C. [Tetrahedron Letters,2020,vol. 61,# 6,art. no. 151471] Location in patent:supporting information

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