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6-methoxy-3,4-dihydronaphthalen-1(2H)-one oximeÔÚ²»Í¬µÄËá¼°ÈܼÁÌõ¼þϽøÐб´¿ËÂü·´Ó¦Ê±£¬×ÜÊǵõ½ÉÙÁ¿µÄ2,3,4,5-tetrahydro-7-methoxy-1H-2-benzazepin-1-one£¬¶øÆäÁíÒ»¸öͬ·ÖÒì¹¹ÌåΪÖ÷²úÎï¡£×î½ü£¬ÎÒÃÇ·¢ÏÖ±´¿ËÂüÖØÅŲúÎïµÄ×é³É·Ö²¼Ëæ×Å·´Ó¦µÄζȺÍʱ¼äÓнϴóµÄ±ä»¯¡£ÎÒÃǺϳɲ¢ÅàÑøÁ˱êÌâÎïÖÊÒÔ±ãÓÚÑо¿·´Ó¦Ìõ¼þ¶ÔÁ½ÖÖͬ·ÖÒì¹¹Ìå²úÎïµÄ±ÈÀýµÄÓ°Ï졣˳·´Ê½¶Ô¼×±½»ÇËáõ¥µÄ±ÈÀý¿ÉÒÔͨ¹ýºË´Å¹²ÕñHÆ×µÄ»ý·ÖÃæ»ýÀ´ÇóµÃ¡£±¾Îı¨µ¼±êÌâÎïÖʵĵ¥¾§½á¹¹¡£ 2,3,4,5-tetrahydro-7-methoxy-1H-2-benzazepin-1-one was always minor product while its another major isomer was 1,3,4,5-tetrahydro-7-methoxy-2H-1-benzazepin-2-one when 6-methoxy-3,4-dihydronaphthalen-1(2H)-one oxime carried out the Beckmann reaction with different acid ang solvent. Recently, we have found the product distribution of the Beckmann rearrangement greatly varied with reaction time and temperature. We synthesized and trained the title compound in order to study the effect of the reaction conditions on the ratio of the two isomers of product. The trans/cis ratio of tosylates was calculated on the basis of NMR integration. In this paper, we report the crystal structure of the title compound. |
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fypiao4989
ľ³æ (Ö°Òµ×÷¼Ò)
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4Â¥2010-08-01 12:12:32
zhjie717
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| 2,3,4,5-tetrahydro-7-methoxy-1H-2-benzazepin-1-one was always minor product while its isomer 1,3,4,5-tetrahydro-7-methoxy-2H-1-benzazepin-2-one the major product when 6-methoxy-3,4-dihydronaphthalen-1(2H)-one oxime carried out the Beckmann reaction with various kinds of acid and solvent. However, we have found the product distribution of the Beckmann rearrangement greatly varied with reaction time and temperature recently. We synthesized and trained the title compound in order to study the effect of the reaction conditions on the ratio of the two isomers of product. The trans/cis ratio of tosylates was calculated on the basis of NMR integration. In this paper, we report the crystal structure of the title compound. |

2Â¥2010-07-31 09:49:54
zhangzws
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|
The Beckmann reaction of 6-methoxy-3,4-dihydronaphthalen-1(2H)-one oxime was carried out under different pH values and solvents. The results shown that little product 2,3,4,5-tetrahydro-7-methoxy-1H-2-benzazepin-1-one was gained and the main product was its another isomer. Recently, it was found from our researcher that the rearrangement product distribution of the Beckmann reaction greatly varied with reaction time and temperature. While, the title compound was synthesized and cultured in order to study the effect on the ratio of the two isomers of the reaction conditions. The trans/cis ratio of tosylates was calculated on the basis of NMR integration. In addition, the crystal structure of the title compound was reported in this paper. ÕâÊÇÎÒУ¶ÔµÄ·Ò룬ÂÛÎÄÖÐÓ¢Óï¶àÓñ»¶¯Óï̬¡£ÁíÍ⣬¥Ö÷ÕâÊÇÄãµÄÕªÒªÂÎÒ¾õµÃÐèÒªÐÞ¸Äһϣ¬ÓеãÂÒ£¬½öÊǽ¨Òé |
3Â¥2010-07-31 10:11:13














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