A kind of new crystal form of anilinoacetonitrile and preparation method thereof
A technology of anilinoacetonitrile and crystal form, which is applied in the field of new crystal form of anilinoacetonitrile and its preparation, can solve the problems of fragile, easy to harden, products with poor flow properties, etc., and achieve small particle size difference, high yield, Good product quality
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Embodiment 1
[0037] In a four-neck flask equipped with a reflux condenser, a thermometer, an agitator, and a constant pressure dropping funnel, add aniline (94.0g, content 99%, 1mol), sodium carbonate (1.1g, content 99%, 0.01mol) , stir and heat to 105°C, add dropwise 50% aqueous solution of hydroxyacetonitrile (119.7g, 1.05mol) between 105°C and 110°C at temperature control, keep warm for 2 hours after the dropwise addition, take samples, analyze the aniline content of 0.7% by GC, stop the reaction , stop stirring, let the reaction solution stand still for 0.5h, separate the organic phase, cool down to 43°C, the organic phase enters the spray cooling device, and cool the spray droplets with cold air at about 8°C countercurrently, and cool for 6-9s to 24 -26°C, collect the cooled solid to obtain 129.6 g of yellow-brown anilinoacetonitrile crystals, with a content of 99.3% and a yield of 97.5%, all in terms of mass percentage.
Embodiment 2
[0039] With the anilinoacetonitrile crystal that embodiment 1 makes, do XRD test:
[0040] The radiation source is a Cu target, the wavelength is 1.54060nm, the scanning angle is 10°-80°, the voltage is 35kV, the current is 25mA, and the scanning speed is 2.4° / min. Its X-ray powder diffraction pattern is as figure 1 shown.
[0041]The crystalline anilinoacetonitrile crystal form has diffraction angles 2θ at 15.440±0.2°, 22.800±0.2°, 24.639±0.2°, 18.368±0.2°, 27.087±0.2°, 31.124±0.2°, 16.684±0.2°, 22.367 There are diffraction peaks at ±0.2°, 28.839±0.2°, and 23.646±0.2°.
[0042] Crystalline anilinoacetonitrile of the present invention, its powder X-ray diagram expresses with interplanar distance D, Bragg angle (2θ), percentage I (%) of relative intensity and intensity (I value) crystal form, as follows:
[0043]
[0044] The differential scanning calorimetry (DSC) diagram of crystalline anilinoacetonitrile figure 2 As shown, its endothermic transition temperature is 47...
Embodiment 3
[0047] A kind of preparation method of anilinoacetonitrile crystal form, adopts following steps:
[0048] Preliminarily cool the organic phase of the anilinoacetonitrile reaction solution obtained in the synthesis process to 50°C; use a spray cooling device to carry out spray cooling and granulation of the organic phase after the preliminary cooling, and pass in 10°C cold air to countercurrently cool the spray droplets , cooled for 16s and cooled to 25°C, collected the cooled solid to obtain yellow-brown crystals, which were identified by the method of Example 2, which was the new crystal form of anilinoacetonitrile of the present invention.
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