Hydroxyl amyl benzoate potassium crystal and preparation method thereof
A technology of hydroxyamylbenzene and potassium formate, applied in the field of medicine, can solve problems such as being unsuitable for large-scale production, high risk, unstable to humidity and the like
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Embodiment 1
[0033] Embodiment 1: Preparation of Potassium Hydroxypentyl Benzoate Crystal III
[0034] Add 10 g of crude potassium hydroxyamyl benzoate into 50 mL of isopropyl ether, heat to reflux to dissolve, cool to room temperature, stir and crystallize for 1 h, filter and dry to obtain 9.3 g of white crystals. The obtained crystal sample is subjected to powder X-ray diffraction, and the obtained collection of illustrative plates is shown in the attached figure 1 , and the spectral data are shown in Table 1.
Embodiment 2
[0035] Embodiment 2: Preparation of Potassium Hydroxypentyl Benzoate Crystal III
[0036] Add 10 g of crude potassium hydroxyamyl benzoate into 100 mL of ethyl acetate, heat to dissolve, cool to 5°C, stir and crystallize for 2 h, filter and dry to obtain 8.5 g of white crystals. The obtained crystal sample is subjected to powder X-ray diffraction, and the obtained collection of illustrative plates is shown in the attached image 3 , and the spectral data are shown in Table 1.
Embodiment 3
[0037] Embodiment 3: Preparation of Potassium Hydroxypentyl Benzoate Crystal III
[0038] Add 10 g of crude potassium hydroxyamyl benzoate into 200 mL of tert-methyl ether, heat to reflux to dissolve, cool to 0°C, stir and crystallize for 2 h, filter and dry to obtain 8.2 g of white crystals. The obtained crystal sample is subjected to powder X-ray diffraction, and the obtained collection of illustrative plates is shown in the attached Figure 5 , and the spectral data are shown in Table 1.
[0039] Table 1 Powder X-ray Diffraction Characteristic Peak Data of Crystal Samples of Examples 1~3
[0040] .
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