USH1223H - Method of making fluorodinitroethanol (fdne) - Google Patents

Method of making fluorodinitroethanol (fdne) Download PDF

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Publication number
USH1223H
USH1223H US07/702,215 US70221591A USH1223H US H1223 H USH1223 H US H1223H US 70221591 A US70221591 A US 70221591A US H1223 H USH1223 H US H1223H
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sub
acid
fdne
cfdnm
reaction
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US07/702,215
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Thomas G. Archibald
Nghi Van Nguyen
Kurt Baum
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US Department of Navy
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US Department of Navy
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/06—Preparation of nitro compounds
    • C07C201/10—Preparation of nitro compounds by substitution of functional groups by nitro groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/06—Preparation of nitro compounds
    • C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups

Definitions

  • This invention relates to a low cost method of making fluorodinitroethanol (FDNE) which is used as a plasticizer and binder in propellants and explosives.
  • FDNE fluorodinitroethanol
  • 1,2-dichlorodifluoroethylene can be purchased commercially or can be prepared in 80% yield from commercially available 1,2-difluorotetrachloroethane by zinc mediated reduction, as taught by E. G. Locke, et al., J. Am. Chem. Society 1934, 56, 1726.
  • the olefin from these sources was found to be an equal mixture of cis and trans isomers of 1,2-difluorotetrachloroethane, contaiminated by 10% of 1,1-difluorodichloroethylene.
  • the source of the unsymmetrical isomer was found to be a 10% impurity of 1,1-difluorotetrachloroethane in the 1,2-difluorotetrachloroethane used as the starting material.
  • the yield of chlorofluoronitroacetic acid in the nitration reaction was increased to 44% by replacing sulfuric acid with oleum.
  • chlorofluoronitroacetic acid was obtained in 63% yield along with 14% of the 1,2-addition product, 1,2-dichloro-1,2-difluoro-2-nitroethyl trifluoroacetate, bringing the total yield of the nitration reaction to 77%.
  • the 1,2-addition product was formed first and then was hydrolyzed in situ, to give the acetic acid derivative.
  • the lower boiling point and diminished water sensitivity of the 1,2-addition product makes it a potentially attractive alternative to chlorofluoronitroacetic acid in subsequent nitration reactions.
  • chlorofluoronitritroacetic is next reacted with fuming nitric acid.
  • nitric acid containing 20% N 2 O 4
  • chlorofluornitronitrosomethane is isolated in 51% yield as an intensely blue liquid by distillation. This intermediate is stable for several days at ambient temperature, but is generally used directly in the next step without further isolation or purification.
  • Chlorofluorodinitromethane can also be prepared by the direct aqueous fluorination of potassium chlorodinitromethane or by the reaction of chlorofluoronitroacetic acid with xenon difluoride.
  • FDNE has been prepared by reduction of fluorotrinitromethane with sodium hydroxide and hydrogen peroxide in the presence of formaldehyde. Attempted reduction of CFDNM under these conditions resulted in substantial hydrolysis to fluoride ion and the formation of small amounts of chlorofluoronitroethanol. Only trace amounts of FDNE were produced in aqueous or aqueous alcohol solvents, However, yields of FDNE as high as 71% were realized when KI was used as the reducing agent. Results using a 30% aqueous ethanolic solution of CFDNM (1 eq), KI (2.3 eq) and 30% formaldehyde solution (1.3 eq) at 70° C. are summarized in the Table IV. Formation of both FDNE and chlorofluoronitroethanol (CFNE) was observed with the maximum amount of FDNE observed at 1 h reaction time.
  • CFNE chlorofluoronitroethanol
  • Chlorofluorodinitromethane from chlorofluoronitronitrosomethane A solution of chlorofluoronitronitrosomethane (3.8 mg, 0.027 mmol) in 0.5 mL of CDCl 3 in an NMR tube was cooled to 5° C. and 0.2 mL of 100% HNO 3 and 0.1 mL of 30% H 2 O 2 solution were added. The temperature was kept at 5° C. until the exothermic reaction subsided. The solution was then shaken at room temperature for 0.5 h until the blue color disappeared. The residue contained 2.5 mg (62% yield) of chlorofluorodinitromethane by 19 F NMR analysis (trifluorotoluene internal standard). This material was identical to authentic chlorofluorodi-nitromethane prepared above.
  • Fluorodinitroethanol from chlorofluorodinitromethane A solution of chlorofluorodinitromethane (0.95 g, 6.0 mmol), KI (2.5 g, 15 mol), and 37% aqueous formaldehyde (0.6 ML, 7 mmol) in 30% aqueous ethanol (10 mL) was heated at 70° C. for 1 h. The solution was cooled and was found to contain 0.62 g (67%) of fluorodinitroethanol and 0.19 g (23%) of chlorofluoronitroethanol by 19 F NMR assay (trifluoroethanol internal standard).

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A method of producing FDNE using readily available fluoroolefins as a fluorine source.

Description

BACKGROUND OF THE INVENTION
1. Field of Invention
This invention relates to a low cost method of making fluorodinitroethanol (FDNE) which is used as a plasticizer and binder in propellants and explosives.
2. Description of Prior Art
Two methods have been used previously for manufacturing fluorodinitroethanol and both have significant difficulties. One was based on the fluorination of nitroform and the other on the fluorination of 2,2-dinitropropanediol (A-diol). Nitroform was available at low cost from Sweden until the supply was curtailed by a plant explosion in the 1970's. Environmental and safety problems still inhibit resumption of the large-scale production of nitroform. In the alternate process, A-diol was deformylated with base and the salt fluorinated. This aqueous fluorination process was complicated by the formation of large amounts of insoluble sodium fluoride, the expense of the A-diol and difficulty in purifying the product. Both of these processes require elemental fluorine, with attendant high plant capital costs.
SUMMARY OF THE INVENTION
In the new process, readily available fluoroolefins are used as the fluorine source for FDNE. Nitration of 1,2-dichlorodifluoroethylene gives chlorofluoronitroacetic acid, and reaction of the latter with red fuming nitric acid gives chlorofluoronitronitrosomethane. Oxidation of chlorofluoronitronitrosomethane gives chlorofluorodinitromethane (CFDNM), and CFDNM is reduced in the presence of formaldehyde to give FDNE. These reactions are summarized below and the preliminary yields are given in Table I.
              TABLE I                                                     
______________________________________                                    
YIELDS OF REACTIONS LEADING TO FDNE                                       
 ##STR1##                                                                 
 ##STR2##                                                                 
 ##STR3##                                                                 
      STARTING                                                            
STEP  MATERIAL     PRODUCT          YIELD                                 
______________________________________                                    
1.    ClFCCFCl     ClFCNO.sub.2 COOH                                      
                                    77%                                   
2.    ClFCNO.sub.2 COOH                                                   
                   ClFCNO.sub.2 NO  52%                                   
3.    ClFCNO.sub.2 NO                                                     
                   ClFC(NO.sub.2).sub.2 (CFDNM)                           
                                    62%                                   
4.    ClFC(NO.sub.2).sub.2                                                
                   FC(NO.sub.2)CH.sub.2 OH (FDNE)                         
                                    71%                                   
______________________________________
DETAILED DESCRIPTION OF THE INVENTION
1,2-dichlorodifluoroethylene can be purchased commercially or can be prepared in 80% yield from commercially available 1,2-difluorotetrachloroethane by zinc mediated reduction, as taught by E. G. Locke, et al., J. Am. Chem. Society 1934, 56, 1726. The olefin from these sources was found to be an equal mixture of cis and trans isomers of 1,2-difluorotetrachloroethane, contaiminated by 10% of 1,1-difluorodichloroethylene. The source of the unsymmetrical isomer was found to be a 10% impurity of 1,1-difluorotetrachloroethane in the 1,2-difluorotetrachloroethane used as the starting material.
The results of the nitration reaction of the 1,2-dichlorodifluoroethylene with various solutions is shown in Table II below. A first solution of 99% nitric acid and 95% sulfuric acid yielded 34% chlorofluoronitroacetic acid.
The yield of chlorofluoronitroacetic acid in the nitration reaction was increased to 44% by replacing sulfuric acid with oleum. When a mixture of oleum, nitric acid and trifluoracetic acid was reacted with 1,2-dichlorodifluoroethylene, chlorofluoronitroacetic acid was obtained in 63% yield along with 14% of the 1,2-addition product, 1,2-dichloro-1,2-difluoro-2-nitroethyl trifluoroacetate, bringing the total yield of the nitration reaction to 77%. Apparently the 1,2-addition product was formed first and then was hydrolyzed in situ, to give the acetic acid derivative. The lower boiling point and diminished water sensitivity of the 1,2-addition product makes it a potentially attractive alternative to chlorofluoronitroacetic acid in subsequent nitration reactions.
              TABLE II                                                    
______________________________________                                    
CHLOROFLUORONITROACETIC ACID                                              
Solvent             Yield                                                 
______________________________________                                    
1.      95% H.sub.2 SO.sub.4                                              
                        34%                                               
        100% HNO.sub.3                                                    
2.      30% Oleum       44%                                               
        100% HNO.sub.3                                                    
3.      30% Oleum, CF.sub.3 COOH                                          
                        77%                                               
        100% HNO.sub.3                                                    
4.      95% H.sub.2 SO.sub.4, CF.sub.3 COOH                               
                        50%                                               
        100% HNO.sub.3, CH.sub.2 Cl.sub.2                                 
5.      (CF.sub.3 CO).sub.2 O, CH.sub.2,Cl.sub.2,                         
                        60%                                               
        100% HNO.sub.3                                                    
______________________________________
The chlorofluoronitritroacetic is next reacted with fuming nitric acid. When the reaction takes place at 80° C. in 90% nitric acid containing 20% N2 O4, chlorofluornitronitrosomethane is isolated in 51% yield as an intensely blue liquid by distillation. This intermediate is stable for several days at ambient temperature, but is generally used directly in the next step without further isolation or purification.
Oxidation of chlorofluoronitronitrosomethane with 30% hydrogen peroxide in nitric acid at ambient temperature gave chlorofluorodinitromethane in 62% isolated yield. The reaction was 90% complete after 15 minutes as shown in Table III.
              TABLE III                                                   
______________________________________                                    
OXIDATION OF                                                              
CHLOROFLUORONITRONITROSOMETHANE TO CFDNM                                  
             ClFC(NO.sub.2)NO                                             
                          ClFC(NO.sub.2).sub.2                            
TIME, MIN    %            %                                               
______________________________________                                    
 0           100          0                                               
15           10.8         56.7                                            
30           8.2          61.7                                            
45           5.1          60.                                             
______________________________________
Chlorofluorodinitromethane can also be prepared by the direct aqueous fluorination of potassium chlorodinitromethane or by the reaction of chlorofluoronitroacetic acid with xenon difluoride.
FDNE has been prepared by reduction of fluorotrinitromethane with sodium hydroxide and hydrogen peroxide in the presence of formaldehyde. Attempted reduction of CFDNM under these conditions resulted in substantial hydrolysis to fluoride ion and the formation of small amounts of chlorofluoronitroethanol. Only trace amounts of FDNE were produced in aqueous or aqueous alcohol solvents, However, yields of FDNE as high as 71% were realized when KI was used as the reducing agent. Results using a 30% aqueous ethanolic solution of CFDNM (1 eq), KI (2.3 eq) and 30% formaldehyde solution (1.3 eq) at 70° C. are summarized in the Table IV. Formation of both FDNE and chlorofluoronitroethanol (CFNE) was observed with the maximum amount of FDNE observed at 1 h reaction time.
              TABLE IV                                                    
______________________________________                                    
REACTION OF CHLOROFLUORO-                                                 
DINITROMETHANE (CFDNM) WITH KI/CH.sub.2 O                                 
 ##STR4##                                                                 
 ##STR5##                                                                 
Time at 70° C.                                                     
             CFDNM    FDNE      CFNE  F                                   
min          %        %         %     %                                   
______________________________________                                    
 0           100      --        --    --                                  
 30          9.0      56.5      18.8  1.8                                 
 60          4.7      66.6      23.8  2.8                                 
 90          3.6      63.1      24.8  4.9                                 
120          3.0      60.2      25.7  4.9                                 
______________________________________
The effect of reaction variables on the yield of the reductive dehalogenation of CFDNM are summarized in Table V, where 19 F NMR is atomic weight 19 floride nuclear magnetic resonance. The reaction with KI was found to be slow at room temperature (RT), with less than 10% of the CFDNM reduced after 3 hours. Reactions conducted at 40° to 75° C. for short periods and then for several days as room temperature gave the best results. When the reaction temperature exceeded 75° C., no FDNE was formed and complete hydrolysis to fluoride ion occurred.
              TABLE V                                                     
______________________________________                                    
REDUCTIVE DEHALOGENATIONS OF CFDNM IN                                     
THE PRESENCE OF FORMALDEHYDE                                              
               Products (Yields from                                      
               .sup.19 F NMR integration)                                 
Protocols        CFDNM    FDNE    CFME  F                                 
______________________________________                                    
H.sub.2 O.sub.2 /NaOH/CH.sub.2 O in water                                 
                 trace    trace    5%   95%                               
0° C., 1 h                                                         
H.sub.2 O.sub.2 /NaOH/CH.sub.2 O                                          
                  5%      none     2%   95%                               
in aq. MeOH                                                               
0° C. for 1 h then RT for 1 h                                      
H.sub.2 O.sub.2 /NaOH/CH.sub.2 O                                          
                 40%      trace   trace 60%                               
in aq. EtOH                                                               
0° C. for 1 h then RT for 1 h                                      
KI/CH.sub.2 O in aq. EtOH                                                 
3 h at RT        90%       5%      5%   none                              
then                                                                      
2 days at RT      8%      50%     34%    5%                               
KI/CH.sub.2 O in aq. EtOH                                                 
2 h at 40° C.                                                      
                 33%      44%     23%   none                              
then                                                                      
2 days at RT     none     71%     29%   trace                             
KI/CH.sub.2 O in aq. EtOH                                                 
1/2 h at 75° C.                                                    
                 15%      58%     24%    3%                               
then                                                                      
2 days at RT     none     67%     30%    3%                               
KI in aq. EtOH   none     none    trace 99%                               
1/2 h at 75° C.                                                    
______________________________________
Small amounts of chlorofluoronitroethanol (CFNE) were observed as a byproduct in most of the KI reductions. The boiling point of CFNE (40° C./0.4 mm) is closed to that of FDNE (41° C./0.1 mm) and these materials could not be separated readily by distillation. Pure chlorofluoronitroethanol was prepared for use as a reference standard by chlorination of 2-fluoro-2-nitro-1,3-propanediol in 45% yield. CFNE was also prepared in small yield by decarboxylation of chlorofluoronitroacetic acid in aqueous formaldehyde.
Reactions of CFDNM with various "soft" nucleophiles and reducing agents are summarized in Table VI below. The best results were obtained with sodium sulfide and sodium thiosulfate. However, sodium sulfide also reacted with formaldehyde to give insoluble trithiane. At room temperature, even after 16 h, these reactions were not complete. The reaction mixture containing sodium thiosulfate gave two phases after it was heated at 70° C. for 10 h. The aqueous phase showed only FDNE and the organic phase showed several unidentified products in addition to FDNE.
              TABLE VI                                                    
______________________________________                                    
REDUCTION OF CFDNM                                                        
Temp        FDNE    CFNE    F    Comments                                 
______________________________________                                    
KBr     RT      --      --         No reaction                            
        70° C.                                                     
                --      --         No reaction                            
CH.sub.3 COOK                                                             
        RT      --      --         No reaction                            
        70° C.                                                     
                --      --         No reaction                            
NaNO.sub.2                                                                
        RT      --      --         No reaction                            
        70° C.                                                     
                --      --         No reaction                            
Na.sub.2 SO.sub.3                                                         
        RT      --      --         No reaction                            
        70° C.                                                     
                --      --         No reaction                            
K.sub.3 Fe(CN).sub.6                                                      
        RT      --      --         No reaction                            
        70° C.                                                     
                --      --         No reaction                            
KOCN    RT      --      --         No reaction                            
        70° C.                                                     
                 2%      5%   16%  Unreacted CFDNM                        
KCN     RT      22%     18%   17%  Unreacted CFDNM                        
        70° C.                                                     
                 7%     50%   40%                                         
Na.sub.2 S.sub.2 O.sub.3                                                  
        RT      60%     trace trace                                       
                                   Unreacted CFDNM                        
KSCN    RT      --      --         No reaction                            
        70° C.                                                     
                35%     trace      Unreacted CFDNM                        
                                   Solid in mixture                       
Na.sub.2 S                                                                
        RT      30%     trace 40%  Unreacted CFDNM                        
        70° C.                                                     
                50%      7%   40%  Water insoluble                        
                                   Solid in mixture                       
______________________________________
Experimental
IR spectra were recorded in CH2 Cl2 on a Perkin-Elmer 700 spectrometer. 1 H, 13 C and 19 F NMR spectra were recorded in CDCl3 on a Brucker AC200 spectrometer and are reported in ppm relative to TMS and FCCl3. Warning: Fluorodinitroethanol is a powerful skin irritant.
Chlorofluoronitroacetic Acid, Sulfuric Acid Procedure. A solution of 100% HNO3 (30 mL) in conc. H2 SO4 (35 mL) was added over 30 min to neat 1,2-dichlorodifluoroethylene (48 g, 0.35 mol) at 10°-15° C.; an exothermic reaction was observed. The mixture was stirred for 10 min at 10° C. The organic layer was separated, and distilled to give 14 g (34%) of chlorofluoronitroacetic acid, bp 45°-65° C. (0.5 mm) (Lit2 bp 90° C./8 mm): 19 F NMR (CDCl3) δ -89.71; 13 C NMR δ113.69 (d, J=303 Hz), 161.21 (d, J=29 Hz).
Chlorofluoronitroacetic Acid, Oleum Procedure. A solution of 100% nitric acid (9 mL) in 30% oleum (11 mL) was added over 25 min to 1,2-dichlorodifluoroethylene (13.3 g, 0.1 mol) at 14°-17° C. The mixture was stirred for 30 min at 10°-14° C. The organic layer was separated, and distilled to give 6.84 g (44%) of chlorofluoronitroacetic acid, bp 80°-85° C. (8 mm), identical to the material prepared above.
Chlorofluoronitroacetic Acid, Oleum-Trifluoroacetic Acid Procedure. A solution of 100% nitric acid (5 mL) and trifluoroacetic acid (4.2 mL, 54 mmol) in 30% oleum (6 mL) was added over 25 min to 1,2-dichlorodifluoroethylene (7.5 g, 56 mmol) at 10°-15° C. The mixture was stirred for 60 min at 10°-14° C. The organic layer was separated, and fractionally distilled to give 2.1 g (14.5%) of 1,2-dichloro-1,2-difluoro-1-nitroethyl trifluoroacetate, as a 50:50 mixture of diasterimers, bp 48°-50° C. (0.5 mm): 19 F NMR (CDCl3 ) δ -76.27 (s, 6 F), -77.50 (s,1 F), -78.49 (s, 1F), -94.37 (s, 1 F), -95.30 (s, 1 F). The second fraction contained 4.0 g of chlorofluoronitroacetic acid, bp 55°-65° C. (0.5 mm), identical to the authentic material prepared above. The oleum layer was heated to 80° C. under vacuum (0.5 mm) to give an additional 1.61 g (63% combined yield) of chlorofluoronitroacetic acid.
Chlorofluoronitronitrosomethane. Red fuming HNO3 (7 mL) was added to a mixture of chlorofluoronitroacetic acid (2.4 g 15.3 mmol) and water (2 mL). The mixture was heated to 100° C. and the distillate boiling at 45°-92° C. was collected until the reaction mixture ceased to be blue in color. The blue distillate contained a mixture of N2 O4 and 1.1 g (51%) of chlorofluoronitronitrosomethane (assayed by 19 F NMR using trifluorotoluene as the internal standard.) 19 F NMR (CDCl3) -85.8 (t, J=10 Hz) (Lit7 -85.6).
Chlorofluorodinitromethane from chlorofluoronitronitrosomethane. A solution of chlorofluoronitronitrosomethane (3.8 mg, 0.027 mmol) in 0.5 mL of CDCl3 in an NMR tube was cooled to 5° C. and 0.2 mL of 100% HNO3 and 0.1 mL of 30% H2 O2 solution were added. The temperature was kept at 5° C. until the exothermic reaction subsided. The solution was then shaken at room temperature for 0.5 h until the blue color disappeared. The residue contained 2.5 mg (62% yield) of chlorofluorodinitromethane by 19 F NMR analysis (trifluorotoluene internal standard). This material was identical to authentic chlorofluorodi-nitromethane prepared above.
Fluorodinitroethanol from chlorofluorodinitromethane. A solution of chlorofluorodinitromethane (0.95 g, 6.0 mmol), KI (2.5 g, 15 mol), and 37% aqueous formaldehyde (0.6 ML, 7 mmol) in 30% aqueous ethanol (10 mL) was heated at 70° C. for 1 h. The solution was cooled and was found to contain 0.62 g (67%) of fluorodinitroethanol and 0.19 g (23%) of chlorofluoronitroethanol by 19 F NMR assay (trifluoroethanol internal standard).
Chlorofluoronitroethanol. A solution of 2-fluoro-2-nitro-1,3-propanediol (3.0 g, 21.6 mol) in of 12.5% bleach (NaCl0, 100 mL) was stirred at ambient temperature for 3 h and then extracted with methylene chloride (2×100 mL). The combined organic solutions were dried (MgSO4) and filtered through a pad of silica gel, and evaporated to give a yellow oil. The residual oil was distilled to give 1.3 g (42%) of chlorofluoronitroethanol, bp 39°-40°0 C. (0.4 mm): 1 H NMR (CDCl3) δ3.58 (b, 1H), 4.16-4.49 (m, 2H); 13 C NMR (CDCl3) δ62.69 (d, J=23.7 Hz), 119.97 (d, J=293.2 Hz); 19 F NMR (CDCl3) δ 98.19 (dd, J=6.8 , 22 Hz). Anal. Calcd for C2 H3 ClFNO3 : C,16.75; H, 2.11; N,9.76. Found: C, 16.72; H, 2.37; N, 9.68.

Claims (5)

We claim:
1. A method of producing fluorodinitroethanol (FDNE) comprising the steps of:
A. Reacting 1,2-dichorodifluoroethylene with a mixture containing a nitrate to obtain chlorofluoronitroacetic acid;
B. reacting said chlorofluoronitroacetic acid with nitric acid to obtain chlorofluoronitronitrosomethane;
C. oxidizing the said chlorofluoronitronitrosomethane to obtain chlorofluorodinitromethane (CFDNM); and
D. reducing said CFDNM in the presence of formaldehyde to produce FDNE.
2. The process of claim 1 in which the initial reaction of 1,2-dichlorofluoroethylene is with a mixture of oleum, nitric acid and trifluoroacetic acid.
3. The process of claim 2 in which said chlorofluoronitronitrosomethane is oxidized with about 30% hydrogen peroxide in nitric acid.
4. The process of claim 3 in which said CFDNM is reduced with KI as the reducing agent.
5. The process of claim 3 in which KI/CH2 O in aquous EtOH is used as the reducing agent for 2 hours at 40° C. and then 2 days at room temperature.
US07/702,215 1991-05-17 1991-05-17 Method of making fluorodinitroethanol (fdne) Abandoned USH1223H (en)

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Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Aqueous Florination of Nitronate Salts J. Org. Chem. 33, No. 8, Aug. 1968, Grakauskas, et al.
Fluoronitroaliphatics-Fluorodinitromethyl Compounds J. Org. Chem. 33, No. Aug. 1968, Kamlet, et al.

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