Organic Syntheses 2003
DOI: 10.1002/0471264180.os034.11
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1,4‐Dinitrobutane

Abstract: 1,4‐Dinitrobutane product: 1,4‐dinitrobutane product: 1,6‐dinitrohexane product: 1,3‐Dinitropropane product: 1,5‐Dinitropentane

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“…), 3a,4c, and (iii) by nitration of the alkyl halides with metal nitrites. For the latter method, silver nitrite in diethyl ether (Victor−Meyer reaction), potassium nitrite, or sodium nitrite in N,N -dimethylformamide (DMF) or in dimethyl sulfoxide (DMSO) (Kornblum reaction) have been frequently used. , The conversion of alkyl halides to nitro compounds is one of the most used methods for the preparation of nitroalkanes; any way, long-reaction times, the use of toxic solvents, and tedious workup are demanded and/or low yields are obtained. Moreover, a further and serious drawback is that the obtained products are usually a mixture, difficult to purify, of the desired nitroalkanes together with the undesired alkyl nitrites.…”
mentioning
confidence: 99%
“…), 3a,4c, and (iii) by nitration of the alkyl halides with metal nitrites. For the latter method, silver nitrite in diethyl ether (Victor−Meyer reaction), potassium nitrite, or sodium nitrite in N,N -dimethylformamide (DMF) or in dimethyl sulfoxide (DMSO) (Kornblum reaction) have been frequently used. , The conversion of alkyl halides to nitro compounds is one of the most used methods for the preparation of nitroalkanes; any way, long-reaction times, the use of toxic solvents, and tedious workup are demanded and/or low yields are obtained. Moreover, a further and serious drawback is that the obtained products are usually a mixture, difficult to purify, of the desired nitroalkanes together with the undesired alkyl nitrites.…”
mentioning
confidence: 99%