A kind of preparation method of β-mercapto carboxylic acid compound
A technology of carboxylic acid compounds and mercapto carboxylic acids, which is applied in chemical instruments and methods, mercaptan preparation, organic compound/hydride/coordination complex catalysts, etc., can solve the problems of harsh reaction conditions and poor catalytic stability, and achieve The effect of high conversion rate, high selectivity and mild reaction conditions
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[0027] The invention provides a kind of preparation method of β-mercapto carboxylic acid compound, comprising:
[0028] Under the action of a solid base catalyst, a solution of hydrogen sulfide and an α, β-unsaturated carboxylic acid compound is subjected to a Michael addition reaction in a reaction solvent to obtain a β-mercapto carboxylic acid compound;
[0029] The solid base catalyst is formed by the condensation reaction of the oxidized carrier compound and ammonia water, or the solid base catalyst is formed by the condensation reaction of the oxidized carrier compound and ammonia derivatives; the carrier compound is selected from polyhydroxy compounds a kind of
[0030] The temperature of the Michael addition reaction is 40-80° C., and the pressure is 0.5-1.0 MPa.
[0031] The solid base catalyst in the present invention has a suitable base strength, which can not only ensure the activation of hydrogen sulfide, promote the reaction, but also inhibit the combination of c...
Embodiment 1
[0068] Add 2.65g (0.0124mol) of sodium periodate and 50mL of water into a 100mL three-neck flask, stir to dissolve the sodium periodate, then add 10g (0.062mol) of cornstarch, control the pH to 3.5, and the temperature is 25°C, after 6 hours of reaction , filtered, washed with water to remove the remaining iodate (detected by starch potassium iodide test paper), then washed the filter cake with ethanol, and dried to obtain oxidized starch (D aldehyde %=39%). Add 10 g (0.062 mol) of the prepared oxidized starch and 50 mL of deionized water into another 100 mL three-necked flask, pass N 2 For protection, add 2.08g (0.030mol) of hydroxylamine hydrochloride, use sodium hydroxide solution to adjust pH=5, heat up to 70°C for 8 hours, and after cooling to room temperature, pour the reaction solution into methanol to precipitate a solid product, filter, and use methanol After washing, it was vacuum dried to obtain a solid base catalyst. The obtained solid base catalyst was compresse...
Embodiment 2
[0070] Add 2.65g (0.0124mol) of sodium periodate and 50mL of water into a 100mL three-necked flask, stir to dissolve the sodium periodate, then add 10g (0.062mol) of microcrystalline cellulose, control pH = 3.5, temperature 25°C, react After 6h, filter, wash with water to remove remaining iodate (detected by starch potassium iodide test paper), then wash the filter cake with ethanol, and dry to obtain oxidized cellulose (D aldehyde %=25%). Add 10 g (0.062 mol) of the prepared oxidized cellulose and 50 mL of deionized water into another 100 mL three-necked flask, pass N 2 For protection, add 2.11g (0.031mol) of ammonia water, use acetic acid to adjust pH=5, heat up to 70°C for 8 hours, cool to room temperature, pour the reaction solution into methanol to precipitate a solid product, filter, wash with methanol, vacuum Dry to obtain a solid base catalyst. The obtained solid base catalyst was compressed and crushed under 15 MPa, and then, regular-shaped particles were selected for...
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