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- ·ÒëEPI: 502
- Ó¦Öú: 8 (Ó×¶ùÔ°)
- ½ð±Ò: 2283.1
- É¢½ð: 5914
- ºì»¨: 32
- Ìû×Ó: 1665
- ÔÚÏß: 321.9Сʱ
- ³æºÅ: 3587652
- ×¢²á: 2014-12-10
- ÐÔ±ð: GG
- רҵ: ¸ß·Ö×Ӻϳɻ¯Ñ§
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Assisson: ½ð±Ò+20, ·ÒëEPI+1, ¡ï¡ï¡ïºÜÓаïÖú 2015-07-28 10:15:32
Assisson: ½ð±Ò+20, ·ÒëEPI+1, ¡ï¡ï¡ïºÜÓаïÖú 2015-07-28 10:15:32
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5-ÂÈ-2-°±»ùÈý·ú¼×±½¹¤ÒÕ·½°¸ Technological Process for 2-Amino-5-chlorobenzotrifluoride 1¡¢²àÁ´ÂÈ»¯£º¼×±½ÔÚ´ß»¯¼Á´æÔÚÏ£¬Í¨ÈëÂÈÆøµÃÈýÂȼױ½¡£ 1,side chain chlorination: With the presence of methylbenzene as catalyst, the trichlorotoluene can be obtained by ventilating chlorine gas 2¡¢·ú»¯£ºÈýÂȼױ½ÔÚ ·ú»¯ÇâºÍ´ß»¯¼Á´æÔÚÏ£¬Éýη´Ó¦µÃÈý·ú¼×±½´Ö²úÆ·£¬³£Ñ¹¾«ÁóµÃÈý·ú¼×±½¡£ 2, Fluorinatio: Under the effect of hydrogen fluoride and catalyst, trichlorotoluene can be reacted into crude trifluorotoluene by increasing reaction temperaturem and then become the refined trifluorotoluene through normal pressure rectification. 3¡¢»·ÂÈ»¯£ºÈý·ú¼×±½ÔÚ ´ß»¯¼ÁµÄ´æÔÚÏ£¬Í¨ÈëÂÈÆø µÃ ¼äÂÈÈý·ú¼×±½´Ö²úÆ·£¬¼õѹ¾«Áó µÃ¼äÂÈÈý·ú¼×±½¡£ 3, Cyclizing chlorination: With the presence of catalyst, the trifluorotoluene can be firstly reacted into crude chlorobenzotrifluoride and then become the refined the product by vacuum distillation 4¡¢Ïõ»¯£º¼äÂÈÈý·ú¼×±½ ÔÚÁòËáÓëÏõËáµÄ´æÔÚÏ£¬³£Î·´Ó¦µÃ 5-ÂÈ-2-Ïõ»ùÈý·ú¼×±½ ´Ö²úÆ·£¬¼õѹ¾«ÁóµÃ³ÉÆ·¡£ 4, nitration: With the presence of sulfuric acid and nitric acid, the chlorobenzotrifluoride will be first reacted into crude 5-chloro-2-nitrobenzotrifluoride under normal temperature, and then become the refined product through vacuum distillation. 5¡¢»¹Ô£º5-ÂÈ-2-Ïõ»ùÈý·ú¼×±½ ÔÚ ¼×´¼ºÍ´ß»¯¼ÁµÄ´æÔÚÏ£¬Í¨ÈëÇâÆøµÄ´Ö²úÆ·£¬»ØÊÕ¼×´¼ºó£¬¼õѹ¾«ÁóµÃ²úÆ·¡£ 5, Reduction reaction: With the presence of methyl alcohol and catalyst, by ventilating hydrogen, firstly the crude 5-chloro-2-nitrobenzotrifluoride can be prepared, then the refined product can be obtained by recycling the waste methyl alcohol within and vacuum distillation. |
2Â¥2015-07-26 20:57:15
hitoli
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- ·ÒëEPI: 7
- Ó¦Öú: 53 (³õÖÐÉú)
- ½ð±Ò: 2585.4
- ºì»¨: 3
- Ìû×Ó: 543
- ÔÚÏß: 151.6Сʱ
- ³æºÅ: 3165981
- ×¢²á: 2014-04-27
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
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Assisson: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-07-28 10:15:51
Assisson: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-07-28 10:15:51
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Technology program for 5-chloro-2-aminotrifluorotoluene 1. chlorizatoin of side-chain: trichlorotoluene is obtained through toluene reacting with chlorine in the presence of catalyst. 2. fluorization: trichlorotoluenen, in the presence of hydrogen fluoride and catalysts, was heated to obtain rude trifluorotoluene, which was distilled to trifluorotoluene under atomosphere. 3. ring chlorination: trifluorotoluene reacted with chlorine in the presence of catalysts to obtain crude meso-chlorotrifluorotoluene, which was distilled to meso-chlorotrifluorotoluene under reduced pressure. 4. nitration: meso-chlorotrifluorotoluene reacted in the presence of sulfuric acid and nitric acid under room temperature to get raw 5-chloro-2-nitrotrifluorotoluene, which was distilled to product under reduced pressure. 5. reduction: 5-chloro-2-nitrotrifluorotoluene reacted with hydrogen in the presence of methanol and catalysts to get raw product, which was distilled to product under reduced pressure after recycle of methanol. |
3Â¥2015-07-26 21:07:42














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