CS274914B2 - Method of alkylsubstituted guanidiniumnitrates preparation - Google Patents
Method of alkylsubstituted guanidiniumnitrates preparationInfo
- Publication number
- CS274914B2 CS274914B2 CS741889A CS741889A CS274914B2 CS 274914 B2 CS274914 B2 CS 274914B2 CS 741889 A CS741889 A CS 741889A CS 741889 A CS741889 A CS 741889A CS 274914 B2 CS274914 B2 CS 274914B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- nitrate
- reaction
- calcium
- alkyl substituted
- alkyl
- Prior art date
Links
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 4
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical class OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 abstract 2
- MVXMNHYVCLMLDD-UHFFFAOYSA-N 4-methoxynaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(OC)=CC=C(C=O)C2=C1 MVXMNHYVCLMLDD-UHFFFAOYSA-N 0.000 abstract 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 239000001569 carbon dioxide Substances 0.000 abstract 2
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 2
- 229940088417 precipitated calcium carbonate Drugs 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- NDEMNVPZDAFUKN-UHFFFAOYSA-N guanidine;nitric acid Chemical class NC(N)=N.O[N+]([O-])=O.O[N+]([O-])=O NDEMNVPZDAFUKN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910017604 nitric acid Inorganic materials 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The mixture obtained by reaction of amine with calcium nitrate in water environment at the temperature of 60 degrees C in presence of carbon dioxide, containing correspondent alkyl substituted ammonium nitrate, or possibly deprived of precipitated calcium carbonate, is mixed and enriched with initial amine, calcium nitrate and once through calcium cyanamide. The reaction mixture is maintained for a period of 1 to 2 hours at a temperature of 60 to 70 degrees C, then it is enriched with carbon dioxide and in hot condition it is deprived of the precipitated calcium carbonate. After cooling the crystallized alkyl substituted guanidine nitrate of the following general formula is isolated from it: R<1> (R<2>) N - C(NH) - NH2 . HNO3, where R<1> means hydrogen or C2 to C4 - alkyl and R<2> means C2 to C4 - alkyl. The remaining water part, containing the corresponding alkyl substituted ammonium nitrate and residua of the resulting dissolved reaction product are returned to another cycle of reaction with calcium cyanamide. The solution can be used for production of some low-toxic insecticides.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CS741889A CS274914B2 (en) | 1989-12-27 | 1989-12-27 | Method of alkylsubstituted guanidiniumnitrates preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CS741889A CS274914B2 (en) | 1989-12-27 | 1989-12-27 | Method of alkylsubstituted guanidiniumnitrates preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
CS741889A2 CS741889A2 (en) | 1991-12-17 |
CS274914B2 true CS274914B2 (en) | 1991-12-17 |
Family
ID=5423270
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CS741889A CS274914B2 (en) | 1989-12-27 | 1989-12-27 | Method of alkylsubstituted guanidiniumnitrates preparation |
Country Status (1)
Country | Link |
---|---|
CS (1) | CS274914B2 (en) |
-
1989
- 1989-12-27 CS CS741889A patent/CS274914B2/en unknown
Also Published As
Publication number | Publication date |
---|---|
CS741889A2 (en) | 1991-12-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR830007671A (en) | Process for the preparation of crystalline 1,1-dioxophenicilanoyloxymethyl 6- (D-α-amino-α-phenylacetamido) phenylanate tosylate hydrate | |
AU579614B2 (en) | Process for the preparation of urea | |
UA7080A1 (en) | Method for producing crystalline thoracemide | |
NO870985L (en) | PROCESS FOR THE MANUFACTURE OF FERTILIZER CONTAINING AMMONIUM NITRATE AND CALCIUM CARBONATE. | |
CS274914B2 (en) | Method of alkylsubstituted guanidiniumnitrates preparation | |
JPS51136623A (en) | Process for preparation of guanidine salts | |
JPS57156449A (en) | Preparation of alpha-amino acid or n-acyl amino acid | |
KR900017999A (en) | Method for preparing tris (2-cyanoethyl) amine | |
RU1810339C (en) | Method of thiourea production | |
JPS5626952A (en) | Water-soluble resin composition | |
JPS56122338A (en) | Preparation of isocyanic acid ester | |
DE3366400D1 (en) | Process for the production of 3-(10,11-dihydro-5h-dibenzo(a,d)-cyclohepten-5-ylidene)-n,n-dimethyl-1-propaneamine-n-oxide | |
JPS57128665A (en) | 3-chloro-4-hydroxy-5-nitrophenylacetic acid amides and their preparation | |
JPS542298A (en) | Production of lime nitrogen | |
WO1995002573A3 (en) | New method for n-cyclopropylation of aromatic amines, as well as compounds and compositions obtained | |
JPS5432420A (en) | Preparation of guanidine carbonate | |
DK583884A (en) | PROCEDURE FOR MAKING A HOME RELATIONSHIP | |
JPS5798272A (en) | Preparation of 5-(2-cyanoethyl)-2,4-imidazolidinedione | |
HU214194B (en) | Process for the preparation of n--dichloracetyl-1-oxa-4-azaspiro-(4,5)-decane | |
GB1062371A (en) | Process for the production of ribonucleotides by fermentation | |
YU46776B (en) | PROCESS OF PRODUCTION OF PURE MONOAMMONIUM-PHOSPHATE BY CONVERSION FROM UREA-PHOSPHATE |