Novel flavor compound and preparation method, application and composition thereof
A compound and composition technology, applied in the field of its preparation method, diketone compound, use and its composition, to achieve the effect of moderate number, many functional groups and low unsaturation
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Embodiment 1
[0026] Embodiment 1: the synthesis of 1-(4-methoxyphenyl)-2,3-butanedione
[0027] Mix 110g of anisaldehyde and 286g of hydroxyacetone at room temperature to obtain a mixture of anisaldehyde and hydroxyacetone; add 63g of 18% hydrochloric acid to the reaction flask, heat up to 50°C, and then add the above-mentioned anise dropwise at a constant speed within 2 hours while stirring The mixture of aldehyde and hydroxyacetone, continue to keep for 2h after dripping;
[0028] Then, 110 g of water was added to the reaction liquid, and the reaction was continued for 2 hours after the temperature was raised to 82° C.; the product was obtained by cooling to 25° C. and filtered, and recrystallized with denatured alcohol to obtain 58.2 g of white crystals. After detection, its melting point is 123.7-123.8°C; the yield is 37.5%.
[0029] 1 H NMR (CDCl 3 , 400MHz): d 2.51(s, 3H), 3.87(s, 3H), 6.46(s, 1H), 6.945(s, 1H), 6.967(s, 1H), 7.22(d, J=1.6Hz, 1H ), 7.81-7.83 (m, 2H) ppm;
[0030...
Embodiment 2
[0032] Embodiment 2: the synthesis of 1-(4-ethoxyphenyl)-2,3-butanedione
[0033] According to Example 1, 1-(4-ethoxyphenyl)-2,3-butanedione can be obtained by using p-ethoxybenzaldehyde with a yield of 32%.
Embodiment 3
[0034] Example 3: Synthesis of 1-(4-hydroxymethoxyphenyl)-2,3-butanedione
[0035] According to Example 1, 1-(4-hydroxymethoxyphenyl)-2,3-butanedione can be obtained by using p-hydroxymethoxybenzaldehyde with a yield of 30%.
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