Method for producing thionocarbamate and dibenzyl disulfide
A technology of dibenzyl disulfide and thiocarbamate, which is applied in the field of preparing thiocarbamate and co-producing dibenzyl disulfide, producing thiocarbamate and dibenzyl disulfide, and can solve problems such as environmental pollution , to achieve high reactivity, increase yield, and avoid waste water and waste gas
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Embodiment 1
[0058] Synthesis of O-isopropyl-N-ethylthiocarbamate and co-production of dibenzyl disulfide:
[0059] 15.16 parts of O-isopropyl-N-ethyl thiocarbamate with a purity of 95.12% and 8.77 parts of sodium isopropyl xanthate with a purity of 90.27% were added to the reactor, fully stirred, and then Add 6.40 parts of benzyl chloride with a purity of 99.0% to the pressure dropping funnel, control the reaction temperature to 75°C, cool to room temperature after 3 hours of reaction, filter to remove sodium chloride, transfer the filtrate to the reactor, and then use a constant pressure dropping funnel to Add 3.34 parts of ethylamine aqueous solution (content: 65% to 70%), heat up to 70°C, react for 2 hours, cool to room temperature, add 0.19 parts of tetra-n-butylammonium iodide (purity: 99.0%) to the reactor, And add 89.27 parts of hydrogen peroxide with a concentration of 2.0% with a constant pressure dropping funnel, stir and react at room temperature for 20 minutes, and the reactio...
Embodiment 2
[0061] Synthesis of O-isopropyl-N-ethylthiocarbamate and co-production of dibenzyl disulfide:
[0062] 30.32 parts of purity of 95.12% O-isopropyl-N-ethyl thiocarbamate and 17.54 parts of purity of 90.27% sodium isopropyl xanthate were added to the reactor, fully stirred, and then Add 12.80 parts of benzyl chloride with a purity of 99.0% to the pressure dropping funnel, control the reaction temperature to 75°C, react for 3 hours and cool to room temperature, filter to remove sodium chloride, transfer the filtrate to the reactor, and then use a constant pressure dropping funnel to Add 6.68 parts of ethylamine aqueous solution (content: 65% to 70%), heat up to 70°C, react for 2 hours, cool to room temperature, add 0.25 parts of tetra-n-butylammonium iodide (purity: 99.0%) into the reactor, Get 11.30 parts of hydrogen peroxide with a concentration of 30%, add 87.11 parts of the separated water phase in Example 1, and add 60.26 parts of distilled water, and add it dropwise to the ...
Embodiment 3
[0064] Synthesis of O-isobutyl-N-ethylthiocarbamate and co-production of dibenzyl disulfide:
[0065] 20.00 parts of O-isobutyl-N-ethylthiocarbamate with a purity of 94.77% and 9.42 parts of sodium isobutyl xanthate with a purity of 91.41% were added to the reactor, fully stirred, and then Add 6.40 parts of benzyl chloride with a purity of 99.0% to the pressure dropping funnel, control the reaction temperature to 65°C, react for 2 hours, cool to room temperature, filter to remove sodium chloride, transfer the filtrate to the reactor, and then use a constant pressure dropping funnel to Add 3.35 parts of ethylamine aqueous solution (content: 65% to 70%), heat up to 70°C, react for 2 hours, cool to room temperature, add 0.48 parts of tetra-n-butylammonium bromide (purity: 99.0%) to the reactor, And add 35.71 parts of 5.0% hydrogen peroxide with a constant pressure dropping funnel, stir and react at room temperature for 20 minutes, and the reaction ends. Stand at room temperature...
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