Preparation method for high-purity opticity bergamio
A technology of linalyl acetate and optical activity, which is applied in the preparation of carboxylic acid esters, chemical instruments and methods, and the preparation of organic compounds. It can solve the problems of unseen research reports and patent applications, and achieve the effect of price increase.
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Embodiment 2
[0014] In this embodiment, when crude linalool is subjected to rectification and fractionation, the vapor pressure of rectification is controlled at 0.35-0.60KPA, the degree of vacuum is 0.07-0.10, the reflux ratio is 1 / 40-60, and the density is between 0.830-0.880. % more than natural linalool. Other process raw materials and conditions are all identical with embodiment 1.
Embodiment 3
[0016] The specific steps of this embodiment are as follows: take natural L-linalool and acetic anhydride with a purity of more than 99% as raw materials, feed them in a ratio of 1:1, and carry out esterification reaction under the catalyst potassium carbonate. The amount of catalyst potassium carbonate is the reactant natural 0.667% of the weight of L-linalool, the reaction temperature is 65-85°C, and the esterification reaction is carried out under reduced pressure (that is, the valve is opened under normal pressure) for 25-35 hours to obtain the product.
Embodiment 4
[0018] The specific steps of this embodiment are as follows: take natural L-linalool and acetic anhydride with a purity of more than 99% as raw materials, feed them in a ratio of 1.4:1, and carry out esterification reaction under the catalyst potassium carbonate. The amount of catalyst potassium carbonate is the reactant natural 0.669% of the weight of L-linalool, the reaction temperature is 65°C, and the esterification reaction is carried out under reduced pressure (that is, the valve is under normal pressure) for 25 to 35 hours to obtain the product.
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Abstract
Description
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