{"id":10463,"date":"2012-09-07T20:34:36","date_gmt":"2012-09-07T20:34:36","guid":{"rendered":"http:\/\/sacheminc.com\/other-chemicals\/tetrabutylammonium-fluoride-tbaf\/"},"modified":"2018-08-17T14:26:05","modified_gmt":"2018-08-17T19:26:05","slug":"%ed%85%8c%ed%8a%b8%eb%9d%bc%eb%b6%80%ed%8b%b8%ec%95%94%eb%aa%a8%eb%8a%84-%eb%b6%88%ed%99%94%eb%ac%bctbaf","status":"publish","type":"page","link":"https:\/\/www.sacheminc.com\/ko\/%ea%b8%b0%ed%83%80-%ed%99%94%ed%95%99%eb%ac%bc%ec%a7%88\/%ed%85%8c%ed%8a%b8%eb%9d%bc%eb%b6%80%ed%8b%b8%ec%95%94%eb%aa%a8%eb%8a%84-%eb%b6%88%ed%99%94%eb%ac%bctbaf\/","title":{"rendered":"\ud14c\ud2b8\ub77c\ubd80\ud2f8\uc554\ubaa8\ub284 \ubd88\ud654\ubb3c(TBAF)"},"content":{"rendered":"<p align=\"left\">SACHEM\uc740 \ud14c\ud2b8\ub77c\ubd80\ud2f8\uc554\ubaa8\ub284 \ubd88\ud654\ubb3c(TBAF)\uc744 \ub2e4\uc74c \uae30\ub2a5\uc744 \uc81c\uacf5\ud558\ub294 3\uc218\ud654\ubb3c \uacb0\uc815\uccb4\ub85c \uc81c\uacf5\ud569\ub2c8\ub2e4.<\/p>\n<ul>\n<li>\ucd5c\uc18c \ud568\uc218\ub7c9(TBAF\uc758 \uac01 \ubab0\uc5d0 \ub300\ud574 \ubb3c\uc758 3\ubab0\ub9cc)<\/li>\n<li>\ub2e4\uc591\ud55c \ubc18\uc751 \uc2dc\uc2a4\ud15c\uc5d0\uc11c \ubc18\uc751\uc131 \uc99d\uac00\ub97c \uc704\ud574 \uc720\uae30 \uc6a9\uc81c\uc5d0\uc11c \uc27d\uac8c \uc6a9\ud574<\/li>\n<li>\uc811\uadfc\uc131 \uc99d\uac00\ub97c \uc704\ud55c \ubd88\uc18c\uc758 &#8220;\ubb34\uc218&#8221; \uc18c\uc2a4(\uc6a9\uc81c\uc5d0\uc11c \uc6a9\ud574\ub418\uace0 \uac74\uc870\ub420 \ub54c)<\/li>\n<li>\uc5fc\uae30 \ucd09\ub9e4 \ubc18\uc751\uc5d0 \uc0ac\uc6a9\ud558\uae30 \uc704\ud55c \ube44\uce5c\ud575\uc131 \uc5fc\uae30<\/li>\n<li>TBDMS (\ud130\ud2b8-\ubd80\ud2f8\ub514\uba54\ud2f8\ud074\ub85c\ub85c\uc2e4\ub780)-\ubcf4\ud638 \uc54c\ucf54\uc62c\uc744 \uc704\ud55c \uac15\ub825\ud55c \ub514\uc2e4\ub9ac\ub808\uc774\uc158 \uc2dc\uc57d<\/li>\n<\/ul>\n<p align=\"left\"><b>\uc751\uc6a9<\/b><b> <\/b><b>\ubd84\uc57c<\/b><b>:<\/b><\/p>\n<ul>\n<li><a title=\"\ub514\uc2e4\ub9ac\ub808\uc774\uc158 \uc2dc\uc57d | Salego\u2122 DSIL\" href=\"\/?page_id=10195\">\ub514\uc2e4\ub9ac\ub808\uc774\uc158 \ub610\ub294 \ub514\ud504\ub85c\ud14d\uc158 \uc2dc\uc57d<\/a><\/li>\n<li><a title=\"\ubc18\ub3c4\uccb4 \ud654\ud559\ubb3c\uc9c8 | Envure\u2122\" href=\"\/?page_id=8085\">\ubc18\ub3c4\uccb4 \ud654\ud559\ubb3c\uc9c8<\/a><\/li>\n<\/ul>\n<p align=\"left\"><b>TBAF <\/b><b>\uc0ac\uc6a9<\/b><b> <\/b><b>\uac00\ub2a5\ud55c<\/b><b> <\/b><b>\uc81c\ud488<\/b><b>:<\/b><\/p>\n<p align=\"left\">\uc2dc\uc124\uacfc \uc644\ubcbd\ud55c \ubb3c\ub958 \uc9c0\uc6d0\uc758 \uae00\ub85c\ubc8c \ub124\ud2b8\uc6cc\ud06c\ub294 \uc804\uc138\uacc4\u2009\uc5b4\ub514\uc11c\ub098 \uc77c\uad00\uc131 \uc788\uace0 \uc548\uc815\uc801\uc774\uace0 \ub2e4\uc591\ud55c \uc218\ub7c9\uc73c\ub85c TBAF\ub97c \uc9c0\uc6d0\ud560 \uc218 \uc788\uc2b5\ub2c8\ub2e4.<\/p>\n<ul>\n<li>\ub300\ub7c9\uc73c\ub85c \uc0c1\uc6a9 \uaddc\ubaa8 \uc81c\uc870 \ub2a5\ub825<\/li>\n<li>TBAF 3\uc218\ud654\ubb3c 25kg \ubc0f 50kg \uc12c\uc720 \ub4dc\ub7fc \ud3ec\uc7a5<\/li>\n<\/ul>\n<p align=\"left\"><b>\ubc31\uc11c<\/b><b>: <\/b><br \/>\nTBAF\uc758 \uc885\ud569 \uc720\ud2f8\ub9ac\ud2f0<a href=\"http:\/\/info.sacheminc.com\/l\/33012\/2014-01-21\/xjy?White_Paper_Requests=Synthetic%20Utility%20of%20TBAF&amp;White_Paper_URL=http:\/\/info.sacheminc.com\/l\/33012\/2014-01-14\/hg9\/33012\/2144\/wp_A_BRIEF_REVIEW_OF_THE_SYNTHETIC_UTILITY_OF_TBAF.pdf\">\ubc31\uc11c \ub2e4\uc6b4\ub85c\ub4dc<\/a><\/p>\n<p align=\"left\"><b>\uc0ac\uc6a9<\/b><b> <\/b><b>\uac00\ub2a5\ud55c<\/b><b> <\/b><b>\uc81c\ud488<\/b><\/p>\n<p align=\"left\"><b>TBAF(<\/b><b>\ud14c\ud2b8\ub77c\ubd80\ud2f8\uc554\ubaa8\ub284<\/b><b> <\/b><b>\ubd88\ud654\ubb3c<\/b><b>) 3<\/b><b>\uc218\ud654\ubb3c<\/b><b>, 98%<\/b><br \/>\nCAS# 87749-50-6<br \/>\n[sachem_product:433]<\/p>\n<p align=\"left\">\ud574\ub2f9 \uc751\uc6a9 \ubd84\uc57c \uc694\uad6c\uc5d0 \ub300\ud574 \ub2f9\uc0ac\uc640 \uc0c1\ub2f4\ud558\uae38 \uc6d0\ud558\uc2ed\ub2c8\uae4c? \ub2f9\uc0ac\uc5d0<a title=\"\uc5f0\ub77d\ucc98\" href=\"\/?page_id=10191\"> \ubb38\uc758\ud558\uc2ed\uc2dc\uc624.<\/a><\/p>\n<p align=\"left\"><b>\ud14c\ud2b8\ub77c\ubd80\ud2f8\uc554\ubaa8\ub284<\/b><b> <\/b><b>\ubd88\ud654\ubb3c\uc758<\/b><b> <\/b><b>\uc120\ud0dd\ub41c<\/b><b> <\/b><b>\uae30\uc0ac<\/b><b> <\/b><b>\ubc0f<\/b><b> <\/b><b>\ud2b9\ud5c8<\/b><b><\/b><\/p>\n<p align=\"left\">[toggle_container keep_open=&#8221;false&#8221; initial_open=&#8221;&#8221;]<br \/>\n[toggle title=&#8221;Click here for selected articles and patents on tetrabutylammonium fluoride.&#8221;]<\/p>\n<p align=\"left\">1. Adam, M. J.; Jivan, S.; Huser, J. M.; Lu, J. (2000).<a href=\"http:\/\/www.xolopo.com\/chemistry\/11c_methylations_11c_methyl_iodide_1077.html\">11C-methylations using 11C-methyl iodide and tetrabutylammonium fluoride<\/a>. Radiochimica Acta (2000), 88(3-4), 207-209.<\/p>\n<p align=\"left\">2. Bartsch, Richard (1970) .\u00a0<a href=\"http:\/\/pubs.acs.org\/cgi-bin\/abstract.cgi\/joceah\/1970\/35\/i04\/f-pdf\/f_jo00829a035.pdf?sessid=6006l3\">Eliminations from 2-butyl halides induced by halide ions in dimethylformamide and dimethyl sulfoxide<\/a>. Journal of Organic Chemistry 35(4), 1023-5.<\/p>\n<p align=\"left\">3. Crawley, Seth and Funk, Raymond. (2006).\u00a0<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/16928057\">Generation of Aza-ortho-xylylenes via Ring Opening of 2-(2- Acylaminophenyl)aziridines: Application in the Construction of the Communesin Ring System<\/a>. Organic Letters 8(18), 3995-3998.<\/p>\n<p align=\"left\">4. Dahlstedt, Emma; Hellberg, Jonas; Petoral, Rodrigo M., Jr.; Uvdal, Kajsa (2004\u00a0<a href=\"http:\/\/www.rsc.org\/publishing\/journals\/JM\/article.asp?doi=b310260b\">Synthesis of tetrathiafulvalenes suitable for self-assembly applications<\/a>. Journal of Materials Chemistry, 14(1), 81-85.<\/p>\n<p align=\"left\">5. Denmark, Scott E; Pan, Weitao. (2003).\u00a0<a href=\"http:\/\/www.scs.uiuc.edu\/denmark\/files\/MS%20213.pdf\">Intramolecular Syn and Anti Hydrosilylation and Silicon-Assisted Cross-Coupling: Highly Regio- and Stereoselective Synthesis of Trisubstituted Allylic Alcohols<\/a>.Organic Letters 5(7), 1119-1122.<\/p>\n<p align=\"left\">6. Hojo, Makoto; Ishibashi, Naruyasu; Hosomi, Akira(1994).\u00a0<a href=\"http:\/\/www3.interscience.wiley.com\/journal\/109568928\/abstract\">Heteroarylthiomethylsilanes. Synthesis and application to heteroarylthiomethylation of carbonyl compounds<\/a>. Heteroatom Chemistry 5(3), 229-34.<\/p>\n<p align=\"left\">7. Lyapkalo, Ilya M.; Webel, Matthias; Reissig, Hans-Ulrich (2001).\u00a0<a href=\"http:\/\/www.thieme-connect.com\/ejournals\/abstract\/synlett\/doi\/10.1055\/s-2001-16058\">Enantioselective synthesis of cyclohexenylalkenes by asymmetric deprotonation of 4-tert-butylcyclohexanone followed by O-nonaflation and Heck couplings<\/a>. Synlett (8), 1293-1295.<\/p>\n<p align=\"left\">8. Muratam Miki; Ohara, Hiroya; Oiwa, Ryo; Watanabe, Shinji; Masuda,Yuzuru (2006).<a href=\"http:\/\/www.thieme-connect.com\/ejournals\/abstract\/synthesis\/doi\/10.1055\/s-2006-942368\">Palladium(0)-catalyzed silylation of aryl halides with triorganosilanes: synthesis of aryl(2-furyl)silanes.<\/a>\u00a0Synthesis, (11), 1771-1774.<\/p>\n<p align=\"left\">9. Ogawa, Toshihisa; Hatayama, Katsuo; Maeda, Hiroshi; Kita, Yasuyuki (1994).\u00a0<a href=\"http:\/\/ci.nii.ac.jp\/naid\/110003631192\/\">Mild and facile cleavage of 2-cyanoethyl ester using sodium sulfide or tetrabutylammonium fluoride. Synthesis of 1,4-dihydropyridine monocarboxylic acids and unsymmetrical 1,4-dihydropyridine dicarboxylates<\/a>. Chemical Pharmaceutical Bulletin 42(8), 1579-89.<\/p>\n<p align=\"left\">10. Ozasa, Nobuko; Wadamoto, Manabu; Ishihara, Kazuaki; Yamamoto, Hisashi (2003).<a href=\"http:\/\/cat.inist.fr\/?aModele=afficheN&amp;cpsidt=15269113\">Aldol synthesis with an aqueous solution of formalin<\/a>. Synlett (14), 2219-2221.<\/p>\n<p align=\"left\">11. Robins, Morris J.; Sarker, Sanchita; Samano, Vicente;.Wnuk, Stanislaw F (1997).\u00a0<a href=\"http:\/\/www.ingentaconnect.com\/content\/els\/00404020\/1997\/00000053\/00000002\/art01035?token=003a1492b41c6720297d76256f7b552b6c7a38385938316d3f4e4b2576\">Nucleic acid related compounds. 94. Remarkably high stereoselective reductions of 2\u2032- and 3\u2032-keto nucleosides to give arabino, ribo, and xylofuranosyl nucleosides with hydrogen isotopes at C2\u2032 and C3\u2032<\/a>. Tetrahedron 53(2), 447-456.<\/p>\n<p align=\"left\">12. Sahoo, Akhila K.; Oda, Takuro; Nakao, Yoshiaki; Hiyama, Tamejiro (2004).\u00a0<a href=\"http:\/\/www3.interscience.wiley.com\/journal\/109858622\/abstract?CRETRY=1&amp;SRETRY=0\">Cross-coupling of triallyl(aryl)silanes with aryl bromides and chlorides: An alternative convenient biaryl synthesis<\/a>. Advanced Synthesis Catalysis 346(13-15), 1715-1727.<\/p>\n<p align=\"left\">13. Shan, Daxian ; Zheng, Ailian; Ballard, C. Eric; Wang, Wei;. Borchardt, Ronald T; Wang, Binghe (2000).\u00a0<a href=\"http:\/\/cat.inist.fr\/?aModele=afficheN&amp;cpsidt=1309691\">A facilitated cyclic ether formation and its potential application in solid-phase peptide and organic synthesis.<\/a>\u00a0Chemical Pharmaceutical Bulletin (2000), 48(2), 238-244.<\/p>\n<p align=\"left\">14. Sekine, Mitsuo; Yamada, Takeshi; Saneyoshi, Hisao; Seio, Kohji (2007). World Patent 2007\/102581.\u00a0<a href=\"http:\/\/www.wipo.int\/pctdb\/en\/fetch.jsp?LANG=ENG&amp;DBSELECT=PCT&amp;SERVER_TYPE=19-10&amp;SORT=41225078-KEY&amp;TYPE_FIELD=256&amp;IDB=0&amp;IDOC=1673011&amp;C=10&amp;ELEMENT_SET=B&amp;RESULT=1&amp;TOTAL=1&amp;START=1&amp;DISP=25&amp;FORM=SEP-0\/HITNUM,B-ENG,DP,MC,AN,PA,ABSUM-ENG&amp;SEARCH_IA=JP2007054533&amp;QUER\">Preparation of 2\u2032-Hydroxyl-Modified Ribonucleoside Derivative<\/a>. World Patent Office.<\/p>\n<p align=\"left\">15. Sharma, G. V. M.; Reddy, V. Goverdhan; Chander, A. Subhash; Reddy, K. Ravinder (2002)\u00a0<a href=\"http:\/\/www.ingentaconnect.com\/content\/els\/09574166\/2002\/00000013\/00000001\/art00047;jsessionid=ba6n0cu3e1j9.alice?format=print\">Tetra-n-butylammonium fluoride: an efficient base for aza-Michael addition-synthesis of glycosyl b-amino acid esters<\/a>. Tetrahedron: Asymmetry 13(1), 21-24.<\/p>\n<p align=\"left\">16. Shiba, Yoshinobu (2007). World Patent 2007\/099896.\u00a0<a href=\"http:\/\/www.wipo.int\/pctdb\/en\/fetch.jsp?LANG=ENG&amp;DBSELECT=PCT&amp;SERVER_TYPE=19-10&amp;SORT=41228238-KEY&amp;TYPE_FIELD=256&amp;IDB=0&amp;IDOC=1700777&amp;C=10&amp;ELEMENT_SET=FILENAME,IMAGEROOT-ENG&amp;RESULT=1&amp;TOTAL=1&amp;START=1&amp;DISP=25&amp;FORM=SEP-0\/HITNUM,B-ENG,DP,MC,AN,PA,ABSUM-ENG&amp;SEARCH\">Method For Detaching Protecting Group On Nucleic Acid<\/a>.\u00a0 World Patent Office.<\/p>\n<p align=\"left\">17. Stawinski, Jacek; Stroemberg, Roger; Thelin, Mats; Westman, Erik (1988).\u00a0<a href=\"http:\/\/www.pubmedcentral.nih.gov\/articlerender.fcgi?artid=338706\">Studies on the t-butyldimethylsilyl group as 2\u2032-O-protection in oligoribonucleotide synthesis via the H-phosphonate approach<\/a>. Nucleic Acids Research 16(19), 9285-98.<\/p>\n<p align=\"left\">18. Tejero, Ismael; Huertas, Imma; Gonzalez-Lafont, Angels; Lluch, Jose M.; Marquet, Jordi (2005).\u00a0<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/15730293\">A Fast Radical Chain Mechanism in the Polyfluoroalkoxylation of Aromatics through NO2 Group Displacement. Mechanistic and Theoretical Studies<\/a>. Journal of Organic Chemistry 70(5), 1718-1727.<\/p>\n<p align=\"left\">[\/toggle]<br \/>\n[\/toggle_container]<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>SACHEM\uc740 \ud14c\ud2b8\ub77c\ubd80\ud2f8\uc554\ubaa8\ub284 \ubd88\ud654\ubb3c(TBAF)\uc744 \ub2e4\uc74c \uae30\ub2a5\uc744 \uc81c\uacf5\ud558\ub294 3\uc218\ud654\ubb3c \uacb0\uc815\uccb4\ub85c \uc81c\uacf5\ud569\ub2c8\ub2e4. \ucd5c\uc18c \ud568\uc218\ub7c9(TBAF\uc758 \uac01 \ubab0\uc5d0 \ub300\ud574 \ubb3c\uc758 3\ubab0\ub9cc) \ub2e4\uc591\ud55c \ubc18\uc751 \uc2dc\uc2a4\ud15c\uc5d0\uc11c \ubc18\uc751\uc131 \uc99d\uac00\ub97c \uc704\ud574 \uc720\uae30 \uc6a9\uc81c\uc5d0\uc11c \uc27d\uac8c \uc6a9\ud574 \uc811\uadfc\uc131 \uc99d\uac00\ub97c \uc704\ud55c \ubd88\uc18c\uc758 &#8220;\ubb34\uc218&#8221; \uc18c\uc2a4(\uc6a9\uc81c\uc5d0\uc11c \uc6a9\ud574\ub418\uace0 \uac74\uc870\ub420 \ub54c) \uc5fc\uae30 \ucd09\ub9e4 \ubc18\uc751\uc5d0 \uc0ac\uc6a9\ud558\uae30 \uc704\ud55c \ube44\uce5c\ud575\uc131 \uc5fc\uae30 TBDMS (\ud130\ud2b8-\ubd80\ud2f8\ub514\uba54\ud2f8\ud074\ub85c\ub85c\uc2e4\ub780)-\ubcf4\ud638 \uc54c\ucf54\uc62c\uc744 \uc704\ud55c \uac15\ub825\ud55c \ub514\uc2e4\ub9ac\ub808\uc774\uc158 \uc2dc\uc57d \uc751\uc6a9 \ubd84\uc57c: \ub514\uc2e4\ub9ac\ub808\uc774\uc158 \ub610\ub294 \ub514\ud504\ub85c\ud14d\uc158 \uc2dc\uc57d &hellip;<\/p>\n","protected":false},"author":43,"featured_media":0,"parent":8164,"menu_order":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-10463","page","type-page","status-publish","hentry","no-thumb"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/www.sacheminc.com\/ko\/wp-json\/wp\/v2\/pages\/10463","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.sacheminc.com\/ko\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.sacheminc.com\/ko\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.sacheminc.com\/ko\/wp-json\/wp\/v2\/users\/43"}],"replies":[{"embeddable":true,"href":"https:\/\/www.sacheminc.com\/ko\/wp-json\/wp\/v2\/comments?post=10463"}],"version-history":[{"count":0,"href":"https:\/\/www.sacheminc.com\/ko\/wp-json\/wp\/v2\/pages\/10463\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/www.sacheminc.com\/ko\/wp-json\/wp\/v2\/pages\/8164"}],"wp:attachment":[{"href":"https:\/\/www.sacheminc.com\/ko\/wp-json\/wp\/v2\/media?parent=10463"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}