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ChemicalBook CAS DataBase List 4-METHOXYCINNAMIC ACID
943-89-5

4-METHOXYCINNAMIC ACID synthesis

12synthesis methods
4-methoxycinnamic acid synthesis : In a 25-mL, roundbottomed flask, 4-methoxybenzaldehyde (0.804 mL, 6.61 mmol) (3), malonic acid (1.75 g, 16.8 mmol), and β-alanine (0.10 g, 1.12 mmol) were dissolved in pyridine (3.0 mL, 37.1 mmol) and heated under reflux for 90 minutes. After cooling to room temperature, the reaction mixture was placed in an ice bath and 8.0 mL of concentrated HCl was slowly added. The resulting white precipitate was collected by vacuum filtration, washed with cold water (2 x 10mL) and dried thoroughly. The product was recrystallized from absolute ethanol (~20 mL).Synthesis of 4-methoxycinnamic acid
Synthesis of 4-methoxycinnamic acid
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Yield:943-89-5 98%

Reaction Conditions:

with piperidine in pyridine for 4 h;Reflux;

Steps:

Synthesis of (E)-3-(4-Methoxyphenyl)acrylic acid (7b)
Malonic acid (1.24 g, 12 mmol) was added to a stirred solution of 6b (1.36 g, 10 mmol), pyridine(6 mL) and piperidine (0.6 mL). The reaction was stirred at reflux for 4 h. The mixture was then cooledto room temperature and poured into a solution of HCl (10 M in H2O, 80 mL) at 0 °C. The white solidthat formed was recovered by filtration and washed with water (200 mL) to afford the title compoundas white powder (1.33g, 98%). 1H NMR (300 MHz, CD3OD) δ 7.62 (d, J = 16.0 Hz, 1H), 7.58-7.47 (m,2H), 7.01-6.88 (m, 2H), 6.33 (d, J = 15.9 Hz, 1H), 3.82 (s, 3H). Data were in accordance with theliterature [28].

References:

Cornelio, Marinonio L.;Jones, Alan M.;Le Duff, Cécile S.;Povinelli, Ana Paula R.;Tang, Bridget;Zazeri, Gabriel [Molecules,2020,vol. 25,# 12]

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