Semicarbazone synthesis method
A technology of semicarbazide and synthesis method is applied in chemical instruments and methods, preparation of urea derivatives, preparation of organic compounds, etc., and can solve the problems of dependence on imports of trimethylsilyl isocyanate, harm to human health, and low level of equipment, etc. To achieve the effect of non-flammable and explosive safety, conducive to industrial production, easy to operate and handle
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Embodiment 1
[0025] Example 1 Synthesis of benzaldehyde semicarbazone in ionic liquid
[0026] Add urea (10g, 0.167mol) and 50% hydrazine hydrate (9g, 0.09mol) successively into a 100mL three-necked round-bottomed flask equipped with a thermometer and a condenser, react at 100°C for 4h, cool to room temperature, and adjust the pH to 3 with concentrated hydrochloric acid. ~4, add dropwise a mixed solution of benzaldehyde (9mL, 0.085mol) and 10mL 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid, a white precipitate is formed immediately, after the addition, stir at room temperature for 2h, Heated to reflux for 1 h, cooled and filtered to obtain white crystals, 12.1 g, yield 95.8%, melting point 220-221 °C. The filtrate was extracted with dichloromethane, and the solvent was evaporated to obtain 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid, which was recycled for use.
Embodiment 2
[0027] Example 2 The synthesis of benzaldehyde semicarbazone under the promotion of ultrasonic waves
[0028] Add urea (10g, 0.167mol) and 50% hydrazine hydrate (9g, 0.09mol) successively into a 100mL three-necked round-bottomed flask equipped with a thermometer and a condenser, react at 95°C for 4h, cool to room temperature, and adjust the pH to 3 with concentrated hydrochloric acid. ~4, dropwise add the mixed solution of benzaldehyde (9mL, 0.085mol) and 10mL 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid, a white precipitate is formed immediately, after the addition, the reaction is accelerated by ultrasonic wave for 0.5 h, heated to reflux for 1 h, cooled and filtered to obtain white crystals, 12.2 g, yield 96.4%, melting point 219-220°C. The filtrate was extracted with dichloromethane, and the solvent was evaporated to obtain 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid, which was recycled for use.
Embodiment 3
[0029] Example 3 Synthesis of benzaldehyde semicarbazone under microwave irradiation
[0030] Add urea (10g, 0.167mol) and 50% hydrazine hydrate (9g, 0.09mol) successively into a 100mL three-necked round-bottomed flask equipped with a thermometer and a condenser, react at 100°C for 4h, cool to room temperature, and adjust the pH to 3 with concentrated hydrochloric acid. ~4, dropwise add the mixed solution of benzaldehyde (9mL, 0.085mol) and 10mL 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid, a white precipitate is formed immediately, after the addition, react under 125W microwave for 10min , cooled and filtered to obtain white crystals, 12.4g, yield 98.0%, melting point 219-222°C. The filtrate was extracted with dichloromethane, and the solvent was evaporated to obtain 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid, which was recycled for use.
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