Process for producing .beta.-nitroenamine

Organic compounds -- part of the class 532-570 series – Organic compounds – Nitriles

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558304, 564384, 564414, 564462, 564485, 564491, 564509, C07C20960, C07C25330

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active

055979408

ABSTRACT:
Disclosed is a process for producing .beta.-nitroenamine represented by the formula I: ##STR1## wherein R.sub.1 and R.sub.2 are the same or different and independently indicate a hydrogen atom or a C.sub.1 -C.sub.10 alkyl group which may be optionally substituted with at least one group selected from the group consisting of a halogen atom, a lower alkoxy group, an aryloxy group, a hydroxyl group or an aryl group, or an aryl group which may be optionally substituted with a halogen atom, a lower alkyl group, a lower alkoxy group, an aryl group, an aryloxy group, a nitro group, a cyano group, an acylamino group, a di-lower alkylamino group, an arylamino group, a hydroxyl group, an arylsulfonyl group, a mercapto group, a lower alkylthio group or an arylthio group, R.sub.1 and R.sub.2 may bond together to form a cycloalkyl or bicycloalkyl and R.sub.3 is a hydrogen atom, a lower alkyl group, a cycloalkyl group or an aralkyl group; and an intermediate for producing the .beta.-nitroenamine.

REFERENCES:
Iimori et al, Tetrahedron Letters, (1979), pp. 2525-2528.
J. Am., Chem., Soc., 78, 1956 The Structure of .beta.-Amino . . . By Jeremiah P. Freeman and William D. Emmons, pp. 3405-3408.
Tokumitsu et al, Nippon Kagaku Kaishi, 1983, pp. 88-93 (abstract).
Rajappa, Tetrahedron, (1981), pp. 1453-1480.
Journal of the American Chemical Society, vol. 75, No. 1, 14 Jan. 1953 DC US, pp. 285-288, Charles D. Hurd et al., The addition of hydroxylamine to omega-nitrostyrene . . . .
Journal of the American Chemical Society, vol. 78, No. 13 7 Jul. 1956 DC US, pp. 3405-3408, Jermiah P. Freeman et al. The structure of Beta-Amino Derivatives . . . .
`Houben-Weyl "Methoden der organischen Chemie" vol. X/1, Part 1, 1971`, George Thieme Verlag, Stuttgart, pp. 399 and 1118.

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