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US4774366A Expired / Lapsed US ⏱️ 0.0 years remaining

Synthesis of geminal dinitro compounds

Assignee: United States Department of the Air Force
•
Filing: 1986-02-24
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Granted: 1988-09-27
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Expires: 2006-02-24
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Abstract

Abstract Geminal dinitro compounds are prepared by reacting an organic nitro compound having a replaceable hydrogen on the carbon to which the nitro group is attached with a source of nitrite ions in the presence of an oxidizing agent and a catalytic amount of an alkali metal ferricyanide.

Inventors

  • 👤 Vytautas Grakauskas
  • 👤 Lee C. Garver
  • 👤 Kurt Baum

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 03:57
CPC Classifications
C; C07; C07D; C07D307/00; C07D307/02; C07D307/26; C07D307/30; C07D307/32; C07D307/33; C07C; C07C201/00; C07C201/06; C07C201/08; C07C205/00; C07C205/01; C07C205/02; C07C205/13; C07C205/14; C07C205/15; C07C205/27; C07C205/28; C07C205/29; C07C205/44; C07C205/49; C07C205/50; C07C205/51; C07D305/00; C07D305/02; C07D305/04; C07D305/08

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 143 words
A process for producing a hydroxy, geminal dinitro compound which comprises reacting an organic nitro compound having a replaceable hydrogen atom attached to the carbon atom to which the nitro group is attached with a C1 to C5 aliphatic aldehyde, and thereafter reacting the resulting nitro-alcohol with a nitrite salt selected from the group consisting of alkali metal nitrites and alkaline earth metal nitrites in the presence of an alkali metal persulfate and about 0.05 to 0.50 moles of an alkali metal ferricyanide per mole of said organic nitro compound, wherein said nitro compound has the general formula ##STR6## wherein R and R' are selected from group consisting of hydrogen, C1 to C4 alkyl, C2 to C6 alkyl ether, C2 to C4 carboxylic acid, C3 to C6 carboxylic acid ester, C6 to C9 cycloalkyl, C7 to C9 aralkyl and C7 to C9 alkaryl.
Claim 2
Dependent Claim 143 words
A process for producing a hydroxy, geminal dinitro compound which comprises reacting an organic nitro compound having a replaceable hydrogen atom attached to the carbon atom to which the nitro group is attached with a C1 to C5 aliphatic aldehyde, and thereafter reacting the resulting nitro-alcohol with a nitrite salt selected from the group consisting of alkali metal nitrites and alkaline earth metal nitrites in the presence of an alkali metal persulfate and about 0.05 to 0.50 moles of an alkali metal ferricyanide per mole of said organic nitro compound, wherein said nitro compound has the general formula ##STR6## wherein R and R' are selected from group consisting of hydrogen, C1 to C4 alkyl, C2 to C6 alkyl ether, C2 to C4 carboxylic acid, C3 to C6 carboxylic acid ester, C6 to C9 cycloalkyl, C7 to C9 aralkyl and C7 to C9 alkaryl.
Claim 3
Dependent Claim 16 words
The process of claim 1 wherein said nitro compound is nitroethane and said aldehyde is formaldehyde.
Claim 4
Dependent Claim 16 words
The process of claim 1 wherein said nitro compound is nitromethane and said aldehyde is formaldehyde.
Claim 5
Dependent Claim 139 words
A process for producing a hydroxy, geminal dinitro compound which comprises reacting an organic nitro compound having a replaceable hydrogen atom attached to the carbon atom to which the nitro group is attached with a nitrite salt selected from the group consisting of alkali metal nitrites in the presence of an alkali metal persulfate and about 0.05 to 0.50 moles of an alkali metal ferricyanide per mole of said organic nitro compound, and thereafter reacting the resulting dinitro compound with a C1 to C5 aliphatic aldehyde, wherein said nitro compound has the general formula ##STR7## wherein R and R' are selected from group consisting of hydrogen, C1 to C4 alkyl, C2 to C6 alkyl ether, C2 to C4 carboxylic acid, C3 to C6 carboxylic acid ester, C6 to C9 cycloalkyl, C7 to C9 aralkyl and C7 to C9 alkaryl.
Claim 6
Dependent Claim 139 words
A process for producing a hydroxy, geminal dinitro compound which comprises reacting an organic nitro compound having a replaceable hydrogen atom attached to the carbon atom to which the nitro group is attached with a nitrite salt selected from the group consisting of alkali metal nitrites in the presence of an alkali metal persulfate and about 0.05 to 0.50 moles of an alkali metal ferricyanide per mole of said organic nitro compound, and thereafter reacting the resulting dinitro compound with a C1 to C5 aliphatic aldehyde, wherein said nitro compound has the general formula ##STR7## wherein R and R' are selected from group consisting of hydrogen, C1 to C4 alkyl, C2 to C6 alkyl ether, C2 to C4 carboxylic acid, C3 to C6 carboxylic acid ester, C6 to C9 cycloalkyl, C7 to C9 aralkyl and C7 to C9 alkaryl.
Claim 7
Dependent Claim 16 words
The processing of claim 4 wherein said nitro compound is nitromethane and said aldehyde is formaldehyde.

References Cited (Backward Citations)

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US2997504A Cited
US3024288A Cited
US3020319A Cited
GB1011115A Cited
US3560575A Cited
US3531534A Cited
US4233250A Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-09-27 1992-03-28 1992-09-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-09-27 1996-03-28 1996-09-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-09-27 2000-03-28 2000-09-27 $7700.00 Window Closed / Lapsed

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