Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2005(1): 33-38
DOI: 10.1055/s-2004-834916
DOI: 10.1055/s-2004-834916
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Methyl (E)-2-Nitromethylcinnamates Derived from Baylis-Hillman Acetates and Conversion into Several Coumarin Derivatives
Further Information
Received
4 August 2004
Publication Date:
17 November 2004 (online)
Publication History
Publication Date:
17 November 2004 (online)
Abstract
Fast and easy access to methyl (E)-2-nitromethylcinnamates, from the corresponding Baylis-Hillman acetates with NaNO2 in DMF is described. Several ortho-chloro-2-nitromethylcinnamates undergo intramolecular aromatic substitution reaction followed by rearrangement to yield coumarin derivatives.
Key words
Baylis-Hillman reaction - sodium nitrite - methyl (E)-2-nitromethylcinnamates - nitronate anion - coumarin
-
1a
Rosini G.Ballini R. Synthesis 1988, 833 -
1b
Ono N. The Nitro Group in Organic Synthesis Wiley-VCH; New York: 2001. -
1c
The Chemistry of Amino, Nitroso, Nitro and Related Groups
Patai S. Wiley; Chichester: 1996. -
1d
Adams JP. J. Chem. Soc., Perkin Trans. 1 2002, 2586 -
1e
Ballini R.Petrini M. Tetrahedron 2004, 60: 1017 - 2
Seebach D.Lehr F. Angew. Chem., Int. Ed. Engl. 1976, 15: 505 - 3
Rosini G. In Comprehensive Organic Synthesis Vol. 2:Trost BM. Pergamon; Oxford: 1991. p.321 - 4
Luzzio FA. Tetrahedron 2001, 57: 915 - 5
Perlmutter P. Conjugate Addition Reactions in Organic Synthesis Pergamon; Oxford: 1992. -
6a
Kim JN.Lee HJ.Lee KY.Gong JH. Synlett 2002, 173 -
6b
Kim JN.Lee HJ.Lee KY.Kim HS. Tetrahedron Lett. 2001, 42: 3737 - 7
Basavaiah D.Kumaragurubaran N.Sharada DS. Tetrahedron Lett. 2001, 42: 85 - 8
Chung YM.Gong JH.Kim TH.Kim JN. Tetrahedron Lett. 2001, 42: 9023 - 9
Lee CH.Song YS.Cho HI.Yang JW.Lee K.-J. J. Heterocycl. Chem. 2003, 40: 1103 -
10a
Basavaiah D.Kumaragurubaran N. Tetrahedron Lett. 2001, 42: 477 -
10b
Im YJ.Kim JM.Mun JH.Kim JN. Bull. Kor. Chem. Soc. 2001, 22: 349 - 11
Drews SE.Horn MM.Ramesar N. Synth. Commun. 2000, 30: 1045 - 12
Foucaud A.El Guemmout F. Bull. Soc. Chim. Fr. 1989, 403 - 13
Basavaiah D.Pandiaraju S. Tetrahedron 1996, 52: 2261 - 14
Patra A.Roy AK.Batra S.Bhaduri AP. Synlett 2002, 1819 - 15
Ko SH.Lee K.-J. J. Heterocycl. Chem. 2004, 41: 613 -
16a
Kim JN.Im YJ.Gong JH.Lee KY. Tetrahedron Lett. 2001, 42: 4195 -
16b
Kim JM.Im YJ.Kim TH.Kim JN. Bull. Kor. Chem. Soc. 2002, 23: 657 -
17a
Chamakh A.Amri H. Tetrahedron Lett. 1998, 39: 375 -
17b
Im YJ.Lee CG.Kim HR.Kim JN. Tetrahedron Lett. 2003, 44: 2987 - 18
Basavaiah D.Hyma RS.Kumaragurubaran N. Tetrahedron 2000, 56: 5905 - 19 For previously reported synthesis of β-nitro acrylic esters by means of NaNO2-CAN mediated conversion of Baylis-Hillman derived acrylic esters, see:
Jayakanthan K.Madhusudanan KP.Vankar YD. Tetrahedron 2004, 60: 397 - For reviews of the Baylis-Hillman reaction, see:
-
20a
Drewes SE.Roos GHP. Tetrahedron 1988, 44: 4653 -
20b
Basavaiah D.Rao PD.Hyma RS. Tetrahedron 1996, 52: 8001 -
20c
Ciganek E. In Organic Reactions Vol. 51:Paquette LA. Wiley; New York: 1997. p.201 -
20d
Langer P. Angew. Chem. Int. Ed. 2000, 39: 3049 -
20e
Kim JN.Lee KY. Curr. Org. Chem. 2002, 6: 627 -
20f
Basavaiah D.Rao AJ.Satyanarayana T. Chem. Rev. 2003, 103: 811 -
21a
Song YS.Lee CH.Lee K.-J. J. Heterocycl. Chem. 2003, 40: 939 -
21b
Park JB.Ko SH.Kim BG.Hong WP.Lee K.-J. Bull. Korean Chem. Soc. 2004, 25: 27 -
21c
Park JB.Ko SH.Hong WP.Lee K.-J. Bull. Kor. Chem. Soc. 2004, 25: 927 -
21d
Lee CH.Lee K.-J. Synthesis 2004, 1941 - 22
Kim JN.Kim HS.Gong JH.Chung YM. Tetrahedron Lett. 2001, 42: 8341 - 23
Murray RDH. In Progress in the Chemistry of Natural ProductsHerz W.Grisebach H.Kirby GW. Springer; New York: 1978. p.199-429 -
24a
von Pechmann H.Duisberg C. Chem. Ber. 1884, 17: 929 -
24b
John EVO.Israelstam SS. J. Org. Chem. 1961, 26: 240 - 25
Panetta JA.Rapoport H. J. Org. Chem. 1982, 47: 946 - 26
Johnson JR. Org. React. 1942, 1: 210 - 27
Shriner RL. Org. React. 1942, 1: 1 - 28
Brufola G.Fringuelli F.Piermatti O.Pizzo F. Heterocycles 1996, 43: 1257 -
29a
Mali RS.Yadav VJ. Synthesis 1977, 464 -
29b
Yavari I.Hekmat-Shoar R.Zonouzi A. Tetrahedron Lett. 1998, 39: 2391 - 30
Yavari I.Djahaniani H.Nasiri F. Synthesis 2004, 679 - 31
Athanasellis G.Melagraki G.Chatzidakis H.Afantitis A.Detsi A.Igglessi-Markopoulou O.Markopoulos J. Synthesis 2004, 1775 - 32
Kotani M.Yamamoto K.Oyamada J.Fujiwara Y.Kitamura T. Synthesis 2004, 1466 -
33a
Kaye PT.Musa MA. Synthesis 2002, 2701 -
33b
Kaye PT.Musa MA.Nocanda XW. Synthesis 2003, 531 - For dihalonitrobenzenes, substitution occurs exclusively at the ortho position of nitro group. See:
-
34a
Parker KA.Coburn CA. J. Org. Chem. 1992, 57: 90 -
34b
Bunnett JF.Morath RJ.Okamoto T. J. Am. Chem. Soc. 1955, 77: 5051 - 36
Keumi T.Matsuura K.Nakayama N.Tsubota T.Morita T.Takahashi I.Kitajima H. Tetrahedron 1993, 49: 537 - 37
Tanaka K.Chen X.Kimura T.Yoneda F. Chem. Pharm. Bull. 1988, 36: 60 -
38a
Mason PH.Emslie ND. Tetrahedron 1994, 50: 12001 -
38b
Nilov D.Räcker R.Reiser O. Synthesis 2002, 2232
References
The stereochemistry of the oximes 7j-n was not determined.