US2941994A - Method for the preparation of hmx using boron trifluoride - Google Patents
Method for the preparation of hmx using boron trifluoride Download PDFInfo
- Publication number
- US2941994A US2941994A US747804A US74780458A US2941994A US 2941994 A US2941994 A US 2941994A US 747804 A US747804 A US 747804A US 74780458 A US74780458 A US 74780458A US 2941994 A US2941994 A US 2941994A
- Authority
- US
- United States
- Prior art keywords
- hmx
- boron trifluoride
- hexamine
- preparation
- added
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 18
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 title claims description 16
- 229910015900 BF3 Inorganic materials 0.000 title claims description 8
- 238000002360 preparation method Methods 0.000 title description 5
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims description 20
- 239000004312 hexamethylene tetramine Substances 0.000 claims description 16
- 235000010299 hexamethylene tetramine Nutrition 0.000 claims description 16
- 238000006243 chemical reaction Methods 0.000 claims description 6
- AOFSUBOXJFKGAZ-UHFFFAOYSA-O azanium nitric acid nitrate Chemical compound [NH4+].O[N+]([O-])=O.[O-][N+]([O-])=O AOFSUBOXJFKGAZ-UHFFFAOYSA-O 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 2
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 29
- UZGLIIJVICEWHF-UHFFFAOYSA-N octogen Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 UZGLIIJVICEWHF-UHFFFAOYSA-N 0.000 description 16
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 239000011541 reaction mixture Substances 0.000 description 8
- 229960000583 acetic acid Drugs 0.000 description 5
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 4
- 239000002360 explosive Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 230000000802 nitrating effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical group [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 2
- ZQXCQTAELHSNAT-UHFFFAOYSA-N 1-chloro-3-nitro-5-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC(C(F)(F)F)=C1 ZQXCQTAELHSNAT-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 238000011031 large-scale manufacturing process Methods 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 229920002866 paraformaldehyde Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- POCJOGNVFHPZNS-ZJUUUORDSA-N (6S,7R)-2-azaspiro[5.5]undecan-7-ol Chemical compound O[C@@H]1CCCC[C@]11CNCCC1 POCJOGNVFHPZNS-ZJUUUORDSA-N 0.000 description 1
- 241001669696 Butis Species 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- BSPUVYFGURDFHE-UHFFFAOYSA-N Nitramine Natural products CC1C(O)CCC2CCCNC12 BSPUVYFGURDFHE-UHFFFAOYSA-N 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000005474 detonation Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- POCJOGNVFHPZNS-UHFFFAOYSA-N isonitramine Natural products OC1CCCCC11CNCCC1 POCJOGNVFHPZNS-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
Definitions
- the present invention relates to the preparation of high explosives of the nitramine type. More particularly the invention pertains to an improved method for the preparation of the explosive known as HMX, in good yield and purity.
- HMX variously known as homocyclonite, cyclotetramethylene tetranitramine, and 1, 3, 5, 7 tetranitro-l, 3, 5, 7 tetraazocyclooctane is known to be an explosive of great power and brisance.
- the detonation rate attainable with HMX strongly suggests the desirability of its use as a military explosive.
- known methods for the preparation of HMX from hexamethylenetetramine '(hexainine) have proven to be unsatisfactory in that the yields obtained were well below the limits of practicality and the product obtained was of inferior quality.
- aprimary object of this invention is the provision of a commercially feasible and more expeditious method of producing homocyclonite.
- a further object of the invention is the provision of a method of preparing homocyclonite from hexamethylenetetramine in good yield and purity with the aid of a suitable catalyst.
- HMX is obtainable in a purity of 80- 86% and an overall yield of 90-96% of theoretical based on the weight of hexamine when the hexamine is treated with nitric acid-ammonium nitrate mixtures of ratios varying from 15:14 to 15:12 in an acid medium consisting of a mixture of acetic anhydride and acetic acid.
- a small quantity of boron trifluoride (from 1 to 15% based on the weight of hexamine) is added to the reaction mixture as a catalyst.
- a small quantity of formaldehyde (0.27 to 0.54 mole equivalent) may be added to the reaction mixture as a means of enhancing the conversion of hexamine to HMX.
- nitrating conditions must be mild in order to obtain good yields of 2,941,994 Patented June 21, 1960 HMX since under stronger conditions of nitration the main reaction product is RDX (cyclonite). It is for this purpose that mild ni-trating conditions have been developed by using a large percentage of ammonium nitrate; by keeping the reaction mixture at relatively low temperatures (40-50 C.) and by using acetic acid as the nitrating medium.
- Example I To a one liter flask, equipped with a stirrer, thermometer and three dropping funnels, were added 125 ml. of glacial acetic acid, 2 ml. of acetic anhydride and 1.6 grams of boron trifluoride. The temperature of the reaction mixture was maintained at 44 :1 C. by means of a water bath. Over a fifteen minute period there was added with constant stirring a solution of 17 grams of hexamine dissolved in 28 grams of glacial acetic acid, 50 ml. acetic anhydride and 20 ml. of a nitric acidammonium nitrate solution via appropriate dropping funnels.
- the nitric acid-ammonium nitrate solution was prepared by dissolving ammonium nitrate in 98% nitric acid in the weight ratio of 15 to 14. This latter solution should be kept above 20 C. to prevent crystallization of the ammonium nitrate from solution.
- the hexamine and nitric acid solution were added continuously and proportionately over the fifteen minute period.
- 8 ml. of acetic anhydride were added to the reaction flask with the exception of the final addition which consisted of 18 ml. of acetic anhydride.
- the reaction mixture was then aged for about 15 minutes. After the aging period, 30 ml.
- nitric acid-ammonium nitrate solution prepared as above, and 30 ml. of acetic anhydride were added continuously and proportionately over a fifteen minute period, followed immediately by a 45 ml. addition of acetic anhydride.
- the reaction mixture was again allowed to age, this time for a period of approximately one hour.
- the reaction mixture was then refluxed with 700 ml. water for a period of thirty minutes, cooled to about 20 C. by the addition of ice, filtered, and the product washed with several portions of cold water and dried.
- the crude yield was 34.2 grams or 95% of theoretical. The purity of the material was approximately -83%.
- Example 2 The same procedure and the same ingredients as recited in Example 1 were employed under the same conditions, Instead :of .employingonly; boron ,trifiuoride as a :cataly'st; however', ,a. 'mixt'ure'gconsisting of 50% V boron trifluoride and 50%. 'paraformaldehydej was used.
- the same procedure and the same ingredients as recited in Example 1 were employed under the same conditions, Instead :of .employingonly; boron ,trifiuoride as a :cataly'st; however', ,a. 'mixt'gconsisting of 50% V boron trifluoride and 50%. 'paraformaldehydej was used.
- the same procedure and the same ingredients as recited in Example 1 were employed under the same conditions, Instead :of .employingonly; boron ,trifiuoride as a :cat
- Example III The same procedure as found in Example I was em- The proportions of the various reactants recited in the i above specific examples are not to be considered as limiting the scope of the process of this invention.
- the mole ratios of nitric acidand ammonium nitrate used to prepare the HMX may be varied from 5 to 7 moles and from 3 to 5 moles respectively per mole of hexamine.
- 'acetic anhydride may be varied in mole ratio between 10 and 11 moles per mole of hexamine.
- the boron trifluoride may be added to the acetic acid-acetic anhydride solution in quantities of from 1 to 15% based on the weight of the hexamine and the formaldehyde in quantities of from 0.27 to 0.54 mole per mole of hexarnine.
Description
United States Patent ,METHOD FOR THE PREPARATION OF HMX USING BORON TRIFLUORIDE r Louis B. Silberman, Keuvil, N.J., assiguor to the United 1 States of America as represented by the Secretary of the Army The invention described herein may be manufactured and used by or for the Government for governmental purposes without the payment to me of any royalties thereon.
The present invention relates to the preparation of high explosives of the nitramine type. More particularly the invention pertains to an improved method for the preparation of the explosive known as HMX, in good yield and purity.
HMX, variously known as homocyclonite, cyclotetramethylene tetranitramine, and 1, 3, 5, 7 tetranitro-l, 3, 5, 7 tetraazocyclooctane is known to be an explosive of great power and brisance. The detonation rate attainable with HMX strongly suggests the desirability of its use as a military explosive. Unfortunately known methods for the preparation of HMX from hexamethylenetetramine '(hexainine) have proven to be unsatisfactory in that the yields obtained were well below the limits of practicality and the product obtained was of inferior quality. The best yields of HMX obtained by the prior art methods were ofthe order of 50-55% or less based on one mole of HMX per mole of hexamethylenetetramine. It will be apparent that the procedures disclosed in the prior art do not lend themselves readily to large scale production.
Accordingly, aprimary object of this invention is the provision of a commercially feasible and more expeditious method of producing homocyclonite.
A further object of the invention is the provision of a method of preparing homocyclonite from hexamethylenetetramine in good yield and purity with the aid of a suitable catalyst.
Other objects and advantages of my invention will be apparent as the invention is hereinafter more particularly described.
I have now found that the foregoing objects may be accomplished by converting hexamethylenetetramine into HMX under mild nitrating conditions and in the presence of a catalyst such as boron trifluoride with or without the presence of a stabilizing agent such as formaldehyde. By means of the use of such stabilizing and catalytic agents it is possible to obtain a product containing 15- 20% more HMX than is possible with prior art methods, thus resulting in a lowering of the cost of manufacturing HMX on large scale production. More specifically I have found that HMX is obtainable in a purity of 80- 86% and an overall yield of 90-96% of theoretical based on the weight of hexamine when the hexamine is treated with nitric acid-ammonium nitrate mixtures of ratios varying from 15:14 to 15:12 in an acid medium consisting of a mixture of acetic anhydride and acetic acid. A small quantity of boron trifluoride (from 1 to 15% based on the weight of hexamine) is added to the reaction mixture as a catalyst. Optionally, a small quantity of formaldehyde (0.27 to 0.54 mole equivalent) may be added to the reaction mixture as a means of enhancing the conversion of hexamine to HMX.
Experimentation has indicated that the nitrating conditions must be mild in order to obtain good yields of 2,941,994 Patented June 21, 1960 HMX since under stronger conditions of nitration the main reaction product is RDX (cyclonite). It is for this purpose that mild ni-trating conditions have been developed by using a large percentage of ammonium nitrate; by keeping the reaction mixture at relatively low temperatures (40-50 C.) and by using acetic acid as the nitrating medium.
The overall reaction involved in this invention may be represented as follows: i
The invention is more specifically illustrated by the following examples in which, as well as throughout the specification, all proportions are given in terms of weight unless specifically stated otherwise.
Example I To a one liter flask, equipped with a stirrer, thermometer and three dropping funnels, were added 125 ml. of glacial acetic acid, 2 ml. of acetic anhydride and 1.6 grams of boron trifluoride. The temperature of the reaction mixture was maintained at 44 :1 C. by means of a water bath. Over a fifteen minute period there was added with constant stirring a solution of 17 grams of hexamine dissolved in 28 grams of glacial acetic acid, 50 ml. acetic anhydride and 20 ml. of a nitric acidammonium nitrate solution via appropriate dropping funnels. The nitric acid-ammonium nitrate solution was prepared by dissolving ammonium nitrate in 98% nitric acid in the weight ratio of 15 to 14. This latter solution should be kept above 20 C. to prevent crystallization of the ammonium nitrate from solution. The hexamine and nitric acid solution were added continuously and proportionately over the fifteen minute period. At the end of each 3-minute period, 8 ml. of acetic anhydride were added to the reaction flask with the exception of the final addition which consisted of 18 ml. of acetic anhydride. The reaction mixture was then aged for about 15 minutes. After the aging period, 30 ml. of nitric acid-ammonium nitrate solution, prepared as above, and 30 ml. of acetic anhydride were added continuously and proportionately over a fifteen minute period, followed immediately by a 45 ml. addition of acetic anhydride. The reaction mixture was again allowed to age, this time for a period of approximately one hour. The reaction mixture was then refluxed with 700 ml. water for a period of thirty minutes, cooled to about 20 C. by the addition of ice, filtered, and the product washed with several portions of cold water and dried. The crude yield was 34.2 grams or 95% of theoretical. The purity of the material was approximately -83%.
The same procedure and the same ingredients as recited in Example 1 were employed under the same conditions, Instead :of .employingonly; boron ,trifiuoride as a :cataly'st; however', ,a. 'mixt'ure'gconsisting of 50% V boron trifluoride and 50%. 'paraformaldehydej was used. The
Although theroleofthe' paraformaldehyde in the .reaction is not fully understood, experimental evidence shows that the presence of the parafor'maldehyde enhances the transformation of the intermediate product DPT into HMX. The formaldehyde may be added either continuously in gaseous form or added all at once in the form of paraformaldehyde at the beginning of the reaction.
Example III The same procedure as found in Example I was em- The proportions of the various reactants recited in the i above specific examples are not to be considered as limiting the scope of the process of this invention. The mole ratios of nitric acidand ammonium nitrate used to prepare the HMX may be varied from 5 to 7 moles and from 3 to 5 moles respectively per mole of hexamine. The
'acetic anhydride may be varied in mole ratio between 10 and 11 moles per mole of hexamine. The boron trifluoride may be added to the acetic acid-acetic anhydride solution in quantities of from 1 to 15% based on the weight of the hexamine and the formaldehyde in quantities of from 0.27 to 0.54 mole per mole of hexarnine.
While the instant invention has been shown and described herein, in what is considered to be themost practical and preferred embfodiments, it is to be recognized that departures may be made therefrom within the scope of the invention, which is therefore not to be limited to the details herein, butis to be accorded the full scope of theclaims so to embrace any and all equivalents.
What is laimed and desired I be securedby United States Letters Patent is:
a process forthe manufacture of homocycloiiite wherein 'hexa'mi'ne is converted to homocyclonite by jtreatment with nitric acid-ammonium nitrate solution inan acidic. medium, the improyement consisting of carrying out the reactionin the presence ofboron trifluoride as a catalyst.
2. :A process for the manufacture of homocyclonite from hexamine as recited in claim 1 wherein said boron .trifluoride is present in amounts ranging from 1.to 15% based on the weight of'the hexamine.
H "3. The process of claim 1 wherein formaldehyde and paraformaldehydeis added to the reaction mixture as a stabilizing agent.
4. The process as recited in claim 1 wherein the temperature is within the range of from 40 to C.
5. The process as recited in claim 1 wherein the acid medium comprises a mixture of acetic acid and acetic anhydride.
' 1 I f References Cited in the file of thispatent UNITED STATES PATENTS 2,67,927 .Wrightet a. May is, 1954 4 2,731,463 Bachmann et al.. Jan. 17,1956
. 2,798,870 Bachmann; July 9, 1957
Claims (1)
1. IN A PROCESS FOR THE MANUFACTURE OF HOMOCYCLONITE WHEREIN HEXAMINE IS CONVERTED TO HOMOCYCLONITE BY TREATMENT WITH NITRIC ACID-AMMONIUM NITRATE SOLUTION IS AN ACIDIC MEDIUM, THE IMPROVEMENT CONSISTING OF CARRYING OUT THE REACTION IN THE PRESENCE OF BORON TRIFLUORIDE AS A CATALYST.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US747804A US2941994A (en) | 1958-07-10 | 1958-07-10 | Method for the preparation of hmx using boron trifluoride |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US747804A US2941994A (en) | 1958-07-10 | 1958-07-10 | Method for the preparation of hmx using boron trifluoride |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2941994A true US2941994A (en) | 1960-06-21 |
Family
ID=25006704
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US747804A Expired - Lifetime US2941994A (en) | 1958-07-10 | 1958-07-10 | Method for the preparation of hmx using boron trifluoride |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2941994A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2983725A (en) * | 1957-11-15 | 1961-05-09 | Jean P Picard | Method for the preparation of hmx |
| US3268588A (en) * | 1962-11-16 | 1966-08-23 | Celanese Corp | Process for producing hexamethylenediamine from 1-6-hexanediol |
| US3360513A (en) * | 1963-06-05 | 1967-12-26 | Union Carbide Corp | Certain esters of azepine carboxylic acids and their preparation |
| US3979379A (en) * | 1975-04-25 | 1976-09-07 | The United States Of America As Represented By The Secretary Of The Army | Process for producing 1,3,5,7-tetraalkanoyl-1,3,5,7-octahydrotetrazocines |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2678927A (en) * | 1944-10-27 | 1954-05-18 | Honorary Advisory Council Sci | Nitramines and their preparation |
| US2731463A (en) * | 1956-01-17 | Manufacture of cyclonite | ||
| US2798870A (en) * | 1943-07-16 | 1957-07-09 | Werner E Bachmann | Method for preparing explosives |
-
1958
- 1958-07-10 US US747804A patent/US2941994A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2731463A (en) * | 1956-01-17 | Manufacture of cyclonite | ||
| US2798870A (en) * | 1943-07-16 | 1957-07-09 | Werner E Bachmann | Method for preparing explosives |
| US2678927A (en) * | 1944-10-27 | 1954-05-18 | Honorary Advisory Council Sci | Nitramines and their preparation |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2983725A (en) * | 1957-11-15 | 1961-05-09 | Jean P Picard | Method for the preparation of hmx |
| US3268588A (en) * | 1962-11-16 | 1966-08-23 | Celanese Corp | Process for producing hexamethylenediamine from 1-6-hexanediol |
| US3360513A (en) * | 1963-06-05 | 1967-12-26 | Union Carbide Corp | Certain esters of azepine carboxylic acids and their preparation |
| US3979379A (en) * | 1975-04-25 | 1976-09-07 | The United States Of America As Represented By The Secretary Of The Army | Process for producing 1,3,5,7-tetraalkanoyl-1,3,5,7-octahydrotetrazocines |
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