Method for synthesizing cholesterol by using stigmasterol degradation products as raw materials
A technology of degradation products, stigmasterol, applied in the field of synthesis of steroids, can solve problems that have not been raised before, and achieve the effects of low production cost, easy industrial implementation, and environmentally friendly process
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Embodiment 1
[0037] The synthesis of embodiment 1 compound (03)
[0038] At room temperature, in a 2000ml glass reaction bottle, add 200ml of ethanol, stir, add 100ml of triethyl orthoformate, add 1g of p-toluenesulfonic acid, add 100g of 3-carbonyl-4-pregna-22-aldehyde (compound 02), Heat to 40°C and keep the reaction for 4 hours. After the reaction was completed, add 1 g of sodium acetate trihydrate, add 1200 ml of water, filter, wash the filter cake with water until the eluate is neutral, drain and dry to obtain 105.82 g of ether compound (compound 03), with a molar yield of 97.50%.
Embodiment 2
[0039] The synthesis of embodiment 2 compound (03)
[0040] The synthesis method is the same as that in Example 1, except that in this example, the consumption of p-toluenesulfonic acid and sodium acetate trihydrate in Example 1 is adjusted to 2g and 2g respectively.
[0041] 105.63 g of compound (03) was obtained with a molar yield of 97.32%.
Embodiment 3
[0042] The synthesis of embodiment 3 compound (03)
[0043] The synthetic method is the same as that in Example 1, except that in this example, the consumption of p-toluenesulfonic acid and sodium acetate trihydrate in Example 1 is adjusted to 4g and 4g respectively.
[0044] 104.69 g of compound (03) was obtained, and the molar yield was 96.46%.
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