Method for interlaminar oxidation of mercaptan compounds by supermolecular structure nanometer reactor
A thiol compound, nano-reactor technology, applied in the preparation of organic compounds, chemical instruments and methods, organic chemistry, etc., can solve the problem of single selectivity of oxidation products
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Embodiment 1
[0024] Step A: 20.48g (0.08mol) of solid Mg(NO 3 ) 2 ·6H 2 O and 15.00g (0.04mol) of solid Al(NO 3 ) 3 9H 2 O dissolved in 50mL to remove CO 2 in deionized water (solution 1); another 10.64g (0.08mol) L-cysteine and 14.08g (0.352mol) NaOH were dissolved in 50mL to remove CO 2 deionized water (solution 2).
[0025] Step B: Place solution 2 in a three-necked flask, under N 2 Under the condition of air protection, while vigorously stirring, solution 1 was slowly added dropwise to solution 2, and the drop was completed in about 2 hours.
[0026] Step C: After the dropwise addition, adjust the pH value to 10 with 5 mol / L NaOH solution, and heat to reflux for 6 hours.
[0027] Step D: CO removal with freshly prepared 2 The deionized hot water was centrifuged and washed to a pH of about 7, and dried at 70°C for 24 hours to obtain a magnesium-aluminum cysteine-intercalated hydrotalcite material.
[0028] According to the XRD spectrum, FT-IR spectrum, thermogravimetric spec...
Embodiment 2
[0032] The preparation method of L-cysteine intercalated hydrotalcite is the same as in Example 1.
[0033] Take 1g of L-cysteine intercalated hydrotalcite, add it to a three-necked bottle, add 50ml 2 Deionized water, N 2 Under protection, stir vigorously for 3h to make it highly dispersed. Then slowly drop a little Br 2 ([Br 2 ] / [CySH]=0.5), after 1 hour of reaction, suction filtration and washing, vacuum drying at room temperature for 48 hours to obtain the oxidized product.
[0034] By XRD, FT-IR, Raman, 13 C NMR and elemental analysis characterization shows that, unlike the open system, due to the influence of the confined space between the hydrotalcite layers, the Br 2 Diffusion becomes more difficult. Br 2 The oxidation product of interlayer cysteine in oxidized hydrotalcite does not change with the amount of oxidant, and the oxidation product is only cysteine sulfonic acid.
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