SU403162A1 - - Google Patents

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Publication number

SU403162A1

SU403162A1 SU47048A SU47048A SU403162A1 SU 403162 A1 SU403162 A1 SU 403162A1 SU 47048 A SU47048 A SU 47048A SU 47048 A SU47048 A SU 47048A SU 403162 A1 SU403162 A1 SU 403162A1

Authority

SU

USSR - Soviet Union

Prior art keywords

carbon atoms

alkyl

salts

formula

nhr

Prior art date

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• 125000004432 carbon atom Chemical group C* 0.000 description 17
• 150000003839 salts Chemical class 0.000 description 9
• 125000000217 alkyl group Chemical group 0.000 description 7
• 150000001875 compounds Chemical class 0.000 description 6
• 238000000034 method Methods 0.000 description 6
• 125000005843 halogen group Chemical group 0.000 description 4
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
• 125000003545 alkoxy group Chemical group 0.000 description 3
• 125000003710 aryl alkyl group Chemical group 0.000 description 3
• -1 nitro, oxy Chemical group 0.000 description 3
• 125000005429 oxyalkyl group Chemical group 0.000 description 3
• 238000002360 preparation method Methods 0.000 description 3
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
• 125000002252 acyl group Chemical group 0.000 description 2
• 125000003342 alkenyl group Chemical group 0.000 description 2
• 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
• 125000004414 alkyl thio group Chemical group 0.000 description 2
• 125000002947 alkylene group Chemical group 0.000 description 2
• 150000001412 amines Chemical class 0.000 description 2
• 125000003118 aryl group Chemical group 0.000 description 2
• 125000004104 aryloxy group Chemical group 0.000 description 2
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
• 125000004093 cyano group Chemical group *C#N 0.000 description 2
• 239000003085 diluting agent Substances 0.000 description 2
• 238000010438 heat treatment Methods 0.000 description 2
• 229910052739 hydrogen Inorganic materials 0.000 description 2
• 239000001257 hydrogen Substances 0.000 description 2
• 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
• 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
• 238000002955 isolation Methods 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• 230000000144 pharmacologic effect Effects 0.000 description 2
• 239000002904 solvent Substances 0.000 description 2
• ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical class C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 1
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
• 229910019142 PO4 Inorganic materials 0.000 description 1
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
• 150000001242 acetic acid derivatives Chemical class 0.000 description 1
• 239000002253 acid Substances 0.000 description 1
• 150000007513 acids Chemical class 0.000 description 1
• 125000003302 alkenyloxy group Chemical group 0.000 description 1
• 125000000304 alkynyl group Chemical group 0.000 description 1
• 150000001408 amides Chemical class 0.000 description 1
• 125000003277 amino group Chemical group 0.000 description 1
• 125000005160 aryl oxy alkyl group Chemical group 0.000 description 1
• 125000004429 atom Chemical group 0.000 description 1
• 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 150000003842 bromide salts Chemical class 0.000 description 1
• 229910052799 carbon Inorganic materials 0.000 description 1
• 150000001805 chlorine compounds Chemical class 0.000 description 1
• 239000002026 chloroform extract Substances 0.000 description 1
• 150000001860 citric acid derivatives Chemical class 0.000 description 1
• 125000000753 cycloalkyl group Chemical group 0.000 description 1
• KSEBMYQBYZTDHS-HWKANZROSA-N ferulic acid Chemical compound COC1=CC(\C=C\C(O)=O)=CC=C1O KSEBMYQBYZTDHS-HWKANZROSA-N 0.000 description 1
• KSEBMYQBYZTDHS-UHFFFAOYSA-N ferulic acid Natural products COC1=CC(C=CC(O)=O)=CC=C1O KSEBMYQBYZTDHS-UHFFFAOYSA-N 0.000 description 1
• 150000004820 halides Chemical class 0.000 description 1
• 125000001188 haloalkyl group Chemical group 0.000 description 1
• 229910052736 halogen Inorganic materials 0.000 description 1
• 150000002367 halogens Chemical class 0.000 description 1
• 230000003993 interaction Effects 0.000 description 1
• 150000003893 lactate salts Chemical class 0.000 description 1
• 150000007522 mineralic acids Chemical class 0.000 description 1
• 150000007524 organic acids Chemical class 0.000 description 1
• 235000005985 organic acids Nutrition 0.000 description 1
• 150000003891 oxalate salts Chemical class 0.000 description 1
• 239000003208 petroleum Substances 0.000 description 1
• 235000021317 phosphate Nutrition 0.000 description 1
• 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
• 150000003873 salicylate salts Chemical class 0.000 description 1
• 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
• 150000003892 tartrate salts Chemical class 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1