Process for preparing thiocarbamate
A technology of thiocarbamate and thiocyanate, which is applied in organic chemistry and other fields, and can solve problems such as high toxicity, strong corrosion, and easy exposure of isothiocyanate
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[0006] A preparation method of thiocarbamate, comprising reacting ammonium thiocyanate with allyl alcohol to generate thiocyanate, then raising the temperature to isomerize thiocyanate into isothiocyanate and distill off excess unreacted Propyl alcohol, and then add another alcohol with a higher boiling point to react with isothiocyanate to generate thiocarbamate. It is characterized in that: thiocyanate is NH 4 SCN; the alcohol reacting with thiocyanate is the alcohol R`OH of propenyl structure, wherein R` is a C3-5 hydrocarbon group; the R of the higher boiling alcohol ROH reacting with isothiocyanate is C3-C8 Alkyl; in the synthesis process, propenyl alcohol R`OH or higher boiling point alcohol ROH or a mixture of the two is used as the solvent medium, and the process is as follows:
[0007] 1. Disperse and dissolve thiocyanate in the mixture of the above-mentioned propenyl alcohol R`OH or R`OH and ROH, and heat up to prepare thiocyanate. The process conditions are:
[00...
Embodiment
[0018] Example 1. Add 2 moles of propenyl alcohol and 0.2 moles of ammonium thiocyanate into the reactor, stir and gradually raise the temperature to reflux the feed solution, and react at 90-100° C. for 3 hours. Then change the reflux to distillation, steam out and recover excess propenyl alcohol. When the temperature rises to 105°C, add 1 mole of isobutanol to the feed liquid, continue distillation, and then add 0.02 mole of catalyst (RO)mTi(Cl)n when the temperature rises to 110°C, (m+n)=4 , react at 110-120°C for 4 hours. Cool and filter, distill off excess alcohol from the filtrate under reduced pressure, and the remaining liquid is 28 grams of thiocarbamate product.
[0019] Example 2, add 1.2 moles of isobutanol, 0.6 moles of propenol, and 0.2 moles of ammonium thiocyanate into the reactor, stir and gradually raise the temperature, make the feed liquid reflux, and react at 90-100° C. for 3 hours. Then change the reflux to distillation, steam out and recover excess prop...
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