SU408475A1 - - Google Patents
Info
- Publication number
- SU408475A1 SU408475A1 SU32393A SU32393A SU408475A1 SU 408475 A1 SU408475 A1 SU 408475A1 SU 32393 A SU32393 A SU 32393A SU 32393 A SU32393 A SU 32393A SU 408475 A1 SU408475 A1 SU 408475A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- tetrahydronaphthalene
- ethano
- cyanomethyl
- ylmethyl
- imidazolin
- Prior art date
Links
- -1 6-chloromethylbenzonorbornan Chemical compound 0.000 description 17
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 150000002462 imidazolines Chemical class 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 229920002866 paraformaldehyde Polymers 0.000 description 2
- 229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ORCQJRXQASSNAQ-UHFFFAOYSA-N 1,8,9,10,11,12-hexahydrotricyclo[6.2.2.0^{2,7}]dodeca-3,9-diene Chemical compound C12=CC=CC=C2C2CCC1CC2 ORCQJRXQASSNAQ-UHFFFAOYSA-N 0.000 description 1
- FLPXXMUNTKLPAP-UHFFFAOYSA-N 2-(4-tricyclo[6.2.2.02,7]dodeca-2(7),3,5-trienyl)acetonitrile Chemical compound N#CCC1=CC2=C(C=C1)C1CCC2CC1 FLPXXMUNTKLPAP-UHFFFAOYSA-N 0.000 description 1
- ZMSBLROJDYNNON-UHFFFAOYSA-N C(C)(C)C12CCC(C3=CC(=CC=C13)CC#N)(CC2)C Chemical compound C(C)(C)C12CCC(C3=CC(=CC=C13)CC#N)(CC2)C ZMSBLROJDYNNON-UHFFFAOYSA-N 0.000 description 1
- QIMPMEMAKMRSLL-UHFFFAOYSA-N CC1=C(C)C(CC#N)=C(C2CCC3CC2)C3=C1 Chemical compound CC1=C(C)C(CC#N)=C(C2CCC3CC2)C3=C1 QIMPMEMAKMRSLL-UHFFFAOYSA-N 0.000 description 1
- YLTZWRZUGAWMKI-UHFFFAOYSA-N CC1=CC2=C(C=C1CC#N)C1CCC2CC1 Chemical compound CC1=CC2=C(C=C1CC#N)C1CCC2CC1 YLTZWRZUGAWMKI-UHFFFAOYSA-N 0.000 description 1
- OYDCLKUPQALFAS-UHFFFAOYSA-N COC1=C(C2CCC3CC2)C3=CC(CC#N)=C1 Chemical compound COC1=C(C2CCC3CC2)C3=CC(CC#N)=C1 OYDCLKUPQALFAS-UHFFFAOYSA-N 0.000 description 1
- BGXFVJFQXIPXAR-UHFFFAOYSA-N COC1=C(CC#N)C=CC2=C1C1CCC2CC1 Chemical compound COC1=C(CC#N)C=CC2=C1C1CCC2CC1 BGXFVJFQXIPXAR-UHFFFAOYSA-N 0.000 description 1
- ZLWULWWXACZTPR-UHFFFAOYSA-N [ClH]=O Chemical compound [ClH]=O ZLWULWWXACZTPR-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- ILMCRZOMKCLIFZ-UHFFFAOYSA-N benzonorbornene Chemical compound C12=CC=CC=C2C2CCC1C2 ILMCRZOMKCLIFZ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- FBBDOOHMGLLEGJ-UHFFFAOYSA-N methane;hydrochloride Chemical compound C.Cl FBBDOOHMGLLEGJ-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU32393A SU59884A1 (ru) | 1940-05-11 | 1940-05-11 | Устройство дл определени ркости вольтовой дуги |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU32393A SU59884A1 (ru) | 1940-05-11 | 1940-05-11 | Устройство дл определени ркости вольтовой дуги |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU32394 Division |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SU408475A1 true SU408475A1 (2) | |
| SU59884A1 SU59884A1 (ru) | 1940-11-30 |
Family
ID=48241890
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU32393A SU59884A1 (ru) | 1940-05-11 | 1940-05-11 | Устройство дл определени ркости вольтовой дуги |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU59884A1 (2) |
-
1940
- 1940-05-11 SU SU32393A patent/SU59884A1/ru active
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