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`¾ËÄÚ¿ÃÀÇ »êÈ­` ¿¹ºñ ½ÇÇ踮Æ÷Æ®ÀÔ´Ï´Ù. ÀÌ·Ð ¹× ½ÇÇè¹æ¹ý±îÁö ±â¼úµÇ¾îÀÖ½À´Ï´Ù.
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1. ½ÇÇè¸ñÀû

2. ÀÌ·Ð

3. ½ÇÇèÀåÄ¡

4. ½ÇÇè¹æ¹ý

5. °á°ú ¹× ÅäÀÇ

º»¹®/³»¿ë
2. ÀÌ·Ð
±¤¹üÀ§ÇÏ°Ô »êÈ­(oxidation)¶õ ¼ö¼Ò¿øÀÚ¸¦ Á¦°ÅÇϰųª »ê¼Ò¿øÀÚ¸¦ ¾ò´Â ¹ÝÀÀÀ»
¸»Çϴµ¥ ÀÌ·¯ÇÑ »êÈ­¹ÝÀÀÀº À¯±âÈ­Çп¡¼­ ³Î¸® ÀÌ¿ëµÇ¾î ¿À°í ÀÖ´Ù. ¾ËÄÚ¿Ã
È­ÇÕ¹°ÀÇ °¡Àå Áß¿äÇÑ ¹ÝÀÀÁßÀÇ Çϳª´Â »êÈ­¿¡ ÀÇÇØ Ä«º¸´Ò(C=O)È­ÇÕ¹°ÀÇ
»ý¼ºÀÌ´Ù. Áï 1Â÷ ¾ËÄÚ¿ÃÀº ¾Ëµ¥È÷µå³ª Ä«¸£º¹½Ç»êÀ» »ý¼ºÇϰí 2Â÷ ¾ËÄÚ¿ÃÀº
ÄÉÅæÀ» »ý¼ºÇÑ´Ù.
1Â÷ ¾ËÄÚ¿ÃÀ» ¾Ëµ¥È÷µå·Î »êÈ­½ÃŰ´Â ¹æ¹ýÀ¸·Î´Â Å©·Ò ±Ý¼ÓÀ» ÀÌ¿ëÇÑ Collins`
regent(CrO3/2pyridine), PCC(C5H6NCrO3(+)/Cl(-)), PDC ((C5H5N)2Cr2O-27(+))
µîÀÌ ÀÖ°í, ±× ¿Ü¿¡µµ MnO2¸¦ ÀÌ¿ëÇÑ ¹æ¹ý°ú Swern(DMSO, (COCl)2, TEA),
Dess-Martin oxdiationµîÀÌ Àß ¾Ë·ÁÁ® ÀÖ´Ù.
1Â÷ ¾ËÄÚ¿ÃÀ» Ä«¸£º¹½Ç»êÀ¸·Î Á÷Á¢ »êÈ­½ÃŰ´Â ¹æ¹ýÀ¸·Î´Â Jones` reagent
(CrO3/H2SO4)°¡ ³Î¸® »ç¿ëµÈ´Ù.
2Â÷ ¾ËÄÚ¿ÃÀ» ÄÉÅæÀ¸·Î »êÈ­½ÃŰ´Â ¹æ¹ýÀ¸·Î´Â sodium dichromate (Na2Cr2O7)³ª
Jones` reagentµîÀÌ »ç¿ëµÇ°í ÀÖ´Ù.
3. ½ÇÇèÀåÄ¡
a. ±â±¸ : µÕ±Ù flask (100mL), Ice bath, Stirrer
b. ½Ã¾à : Citronellol (560mg), Pyridine (3.6mL), 2N-HCl, Celite, TLC plate¿Í
Chamber

4. ½ÇÇè¹æ¹ý
[CitronellolÀÇ »êÈ­]
1¡¦(»ý·«)
Âü°í¹®Çå
o McMurry, `Organic Chemistry, `Brooks/Cole Publishing Company,
1996 (4th ed.).
o Fessenden, `Organic Chemistry, `Brooks/Cole Publishing Company,
1993 (5th ed.).
o Carruthers, `Some Modern Methods of Organic Synthesis,` Cambridge
University Press, 1986 (3th ed.).
o Smith, `Organic Synthesis,` McGraw-Hill International Editions, 1994.



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Date : 2012-06-20
FileNo : 16039195

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