13 C NMR
Organic Chemists from Industry and academics to Interact on Spectroscopy Techniques for Organic Compounds ie NMR, MASS, IR, UV Etc. Starters, Learners, advanced, all alike, contains content which is basic or advanced, by Dr Anthony Melvin Crasto, Worlddrugtracker, email me ........... amcrasto@gmail.com, call +91 9323115463 India skype amcrasto64
................DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 25Yrs Exp. in the feld of Organic Chemistry,Working for GLENMARK GENERICS at Navi Mumbai, INDIA. Serving chemists around the world. Helping them with websites on Chemistry.Million hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contribution
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Tuesday, 1 December 2015
6 ETHYL 4 HYDROXY 2 PYRONE
13 C NMR
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3-Methyl-1-hexen-5-yn-3-ol
3-Methyl-1-hexen-5-yn-3-ol
b.p. 54-55°/25 mm, nD22 1.4576, d425 0.8930.
Ir (neat film) 3400(s, OH stretch), 3300(s, alkyn C-H stretch), 3040(m,=C-H stretch),2950(m), 2930(m), 2910(m), 2120(w), 1640(m, C=C stretch), 1450(m), 1410(s), 1370 (s, CH3), 1270(m), 1240(m), 1170(m), 1110(s), 995(m), 920(s), 870(m), 760(m), 750(m), and 650(v.s.) cm-1.
1H Nmr (60MHz, CDCl3) δ, singlet at 1.40 (3H, Methyl), a doublet at 2.45, (2H, aliphatics), a broad singlet at 3.35,1H, hydroxyl), a doublet of doublets centered at 5.10 and 5.30 (total 2H, terminal vinyl), and a doublet of doublets at 6.10(1H, internal vinyl).
DOI: 10.1021/ja00861a029
2) A. Viola and J.H. MacMillan, J. Amer. Chem. Soc., 90, 6141, (1968).
DOI: 10.1021/ja01024a035
3) Triple Bond Participation in the Oxy-Cope Rearrangement", John H. MacMillan, Ph.D. Thesis, Northeastern University, 1970, Dissertation Abstracts International, Order Number 72-13,297. http://dissexpress.umi.com/dxweb/results.html?QryTxt=&By=John+Harry+MacMillan&Title=&pubnum=7213297
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Ir (neat film) 3400(s, OH stretch), 3300(s, alkyn C-H stretch), 3040(m,=C-H stretch),2950(m), 2930(m), 2910(m), 2120(w), 1640(m, C=C stretch), 1450(m), 1410(s), 1370 (s, CH3), 1270(m), 1240(m), 1170(m), 1110(s), 995(m), 920(s), 870(m), 760(m), 750(m), and 650(v.s.) cm-1.
1H Nmr (60MHz, CDCl3) δ, singlet at 1.40 (3H, Methyl), a doublet at 2.45, (2H, aliphatics), a broad singlet at 3.35,1H, hydroxyl), a doublet of doublets centered at 5.10 and 5.30 (total 2H, terminal vinyl), and a doublet of doublets at 6.10(1H, internal vinyl).
1) Alfred Viola and John H.
MacMillan, "A Novel Steric Effect in the Thermolysis of Prop-2-ynyl
Vinyl Carbinols" Chemical Communications, p 301, (1970). DOI: 10.1039/C29700000301
1) F. Sondheimer, Y. Amiel, and Y. Gaoni, J. Amer. Chem. Soc., 84, 270-274, (1962).
DOI: 10.1021/ja00861a029
2) A. Viola and J.H. MacMillan, J. Amer. Chem. Soc., 90, 6141, (1968).
DOI: 10.1021/ja01024a035
3) Triple Bond Participation in the Oxy-Cope Rearrangement", John H. MacMillan, Ph.D. Thesis, Northeastern University, 1970, Dissertation Abstracts International, Order Number 72-13,297. http://dissexpress.umi.com/dxweb/results.html?QryTxt=&By=John+Harry+MacMillan&Title=&pubnum=7213297
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