Preparation for p-benzoquionone dioxime
A technology of p-benzoquinone dioxime and p-benzoquinone, which is applied in oxime preparation, organic chemistry and other directions, can solve the problems of complicated steps, sewage discharge in the synthesis process, product purity limitation, etc., and achieves high reaction yield, high product purity, and waste. The effect of less liquid discharge
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Embodiment 1
[0012] In the first step, put 4.0g of p-benzoquinone, 5.4g of calcium carbonate, and 10.0g of hydroxylamine chloride into the reactor, add 80ml of ethanol and 20ml of water, and stir evenly. React at 70° C. for 3 h. After the reaction is complete, the product is evaporated in vacuo to remove the solvent.
[0013] In the second step, add 60ml of water and 11.3g of hydrochloric acid with a mass fraction of 36.5% into the container after removing the solvent, stir evenly for 5min, then filter the product with suction, wash with water, and dry to obtain 4.05g of the product. Through high-performance liquid chromatography analysis, compared with the standard sample, the product purity reaches more than 99%. The target product yield was 79.2%.
Embodiment 2
[0015] In the first step, put 4.0g of p-benzoquinone, 4.1g of calcium carbonate, and 10.0g of hydroxylamine chloride into the reactor, add 80ml of ethanol and 20ml of water, and stir evenly. React at 70° C. for 3 h. After the reaction is complete, the product is evaporated in vacuo to remove the solvent.
[0016] In the second step, add 60ml of water and 11.3g of hydrochloric acid with a mass fraction of 36.5% into the container after removing the solvent, stir evenly for 5min, then filter the product with suction, wash with water, and dry to obtain 4.49g of the product. Through high-performance liquid chromatography analysis, compared with the standard sample, the product purity reaches more than 99%. The target product yield was 87.9%.
Embodiment 3
[0018] In the first step, put 4.0g of p-benzoquinone, 3.4g of calcium carbonate, and 10.0g of hydroxylamine chloride into the reactor, add 80ml of ethanol and 20ml of water, and stir evenly. React at 70° C. for 3 h. After the reaction is complete, the product is evaporated in vacuo to remove the solvent.
[0019] In the second step, add 60ml of water and 11.3g of hydrochloric acid with a mass fraction of 36.5% into the container after removing the solvent, stir evenly for 5 minutes, then filter the product with suction, wash with water, and dry to obtain 4.77g of the product. Through high-performance liquid chromatography analysis, compared with the standard sample, the product purity reaches more than 99%. The target product yield was 93.3%.
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