Compound with cinnamon aroma and preparation method and application thereof
A compound and aroma technology, which is applied in the field of compounds with cinnamon aroma and preparation thereof, can solve the problems of easy oxidative deterioration, complex original plants, and difficulty in cinnamon, and achieves the effects of strong and lasting aroma, rich sources, and not easy to deteriorate.
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[0100] The compounds with cinnamon aroma and the preparation method thereof of the present invention are exemplified below. It can be understood that the compounds with cinnamon aroma and the preparation method thereof of the present invention are not limited to the following examples.
[0101] In the description of the present invention, it should be understood that the terms "first" and "second" are only used for description purposes, and cannot be interpreted as indicating or implying relative importance or implying the number of indicated technical features. Thus, a feature defined as "first" or "second" may expressly or implicitly include one or more of that feature. In the description of the present invention, "plurality" means two or more, unless otherwise expressly and specifically defined.
[0102] The weight of the relevant components mentioned in the description of the embodiment of the present invention can not only refer to the specific content of each component, ...
Embodiment 1
[0104] The preparation process with the cinnamon aroma compound of the present embodiment is as follows:
[0105] 1) preparation of 4-methoxyacetophenone:
[0106]
[0107]Add 66.7 g (0.5 mol) of aluminum trichloride and 39.3 g (0.5 mol) of acetyl chloride to the round-bottomed flask in turn, slowly add 162.2 g (1.5 mol) of anisole dropwise, and heat under reflux for 2 hours after the dropwise addition. After the reaction, cooled to room temperature, evaporated anisole under reduced pressure, slowly poured into 200 g of warm water, extracted with dichloromethane (200 mL×3), combined the organic phases, washed with water, and dried over anhydrous sodium sulfate. After filtration, dichloromethane was evaporated under reduced pressure, dried and cooled to obtain 4-methoxyacetophenone (58.6g) as a pale yellow crystal product.
[0108] 2) Preparation of 2-(4-methoxy)-phenyl-2-butanol:
[0109]
[0110] Add 45.4g (0.3mol) of 4-methoxyacetophenone, 14.6g (0.6mol) of polished ...
Embodiment 2
[0126] The preparation process with the cinnamon aroma compound of the present embodiment is as follows:
[0127] 1) preparation of 4-methoxyacetophenone:
[0128] Add 66.7 g (0.5 mol) of aluminum trichloride and 39.3 g (0.5 mol) of acetyl chloride to the round-bottomed flask in turn, slowly add 162.2 g (1.5 mol) of anisole dropwise, and heat under reflux for 2 hours after the dropwise addition. After the reaction, cooled to room temperature, evaporated anisole under reduced pressure, slowly poured into 200 g of warm water, extracted with dichloromethane (200 mL×3), combined the organic phases, washed with water, and dried over anhydrous sodium sulfate. After filtration, dichloromethane was evaporated under reduced pressure, dried and cooled to obtain 4-methoxyacetophenone (58.6g) as a pale yellow crystal product.
[0129] 2) Preparation of 2-(4-methoxy)-phenyl-2-butanol:
[0130] Add 45.4g (0.3mol) of 4-methoxyacetophenone, 14.6g (0.6mol) of polished and shredded magnesium ...
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