DE248777A - - Google Patents

Info

Publication number

DE248777A

DE248777A DE248777A DE 248777 A DE248777 A DE 248777A DE 248777 A DE248777 A DE 248777A

Authority

DE

Germany

Prior art keywords

acid

phenyl

acids

derivatives

ether

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.)

Pending

Links

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• 239000002253 acid Substances 0.000 claims description 8
• 150000001408 amides Chemical class 0.000 claims description 6
• 150000007513 acids Chemical class 0.000 claims description 5
• SHDBWXXRCCHGQD-UHFFFAOYSA-N 2-methyl-2-(4-methylphenyl)propanoic acid Chemical compound CC1=CC=C(C(C)(C)C(O)=O)C=C1 SHDBWXXRCCHGQD-UHFFFAOYSA-N 0.000 claims description 2
• 125000000217 alkyl group Chemical group 0.000 claims description 2
• 125000003118 aryl group Chemical group 0.000 claims description 2
• 238000000034 method Methods 0.000 claims description 2
• 238000002360 preparation method Methods 0.000 claims description 2
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
• -1 phenyl diethylacetylurea Chemical compound 0.000 description 5
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
• DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 3
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
• PYXQBGGQMBEYLO-UHFFFAOYSA-N 2-ethyl-2-phenylbutanoic acid Chemical compound CCC(CC)(C(O)=O)C1=CC=CC=C1 PYXQBGGQMBEYLO-UHFFFAOYSA-N 0.000 description 2
• VZFHOKANOVYGHO-UHFFFAOYSA-N 2-phenyl-2-propylpentanenitrile Chemical compound CCCC(CCC)(C#N)C1=CC=CC=C1 VZFHOKANOVYGHO-UHFFFAOYSA-N 0.000 description 2
• DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
• 239000004471 Glycine Substances 0.000 description 2
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
• 238000009835 boiling Methods 0.000 description 2
• 239000004202 carbamide Substances 0.000 description 2
• 230000000147 hypnotic effect Effects 0.000 description 2
• 238000002844 melting Methods 0.000 description 2
• 230000008018 melting Effects 0.000 description 2
• 150000002825 nitriles Chemical class 0.000 description 2
• 239000003208 petroleum Substances 0.000 description 2
• QHQWYLVUSIWEDA-UHFFFAOYSA-N 2-(2-phenylethyl)pentanoic acid Chemical compound CCCC(C(O)=O)CCC1=CC=CC=C1 QHQWYLVUSIWEDA-UHFFFAOYSA-N 0.000 description 1
• VMWAPTXFNZLIEZ-UHFFFAOYSA-N 2-ethyl-2-phenylbutanoyl chloride Chemical compound CCC(CC)(C(Cl)=O)C1=CC=CC=C1 VMWAPTXFNZLIEZ-UHFFFAOYSA-N 0.000 description 1
• ABNUAFDYCOJGOZ-UHFFFAOYSA-N 2-methyl-2-(4-methylphenyl)propanamide Chemical compound CC1=CC=C(C(C)(C)C(N)=O)C=C1 ABNUAFDYCOJGOZ-UHFFFAOYSA-N 0.000 description 1
• RINQAFSDAWYOFT-UHFFFAOYSA-N 2-phenyl-2-propylpentanoic acid Chemical compound CCCC(CCC)(C(O)=O)C1=CC=CC=C1 RINQAFSDAWYOFT-UHFFFAOYSA-N 0.000 description 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
• 229910021529 ammonia Inorganic materials 0.000 description 1
• 230000001754 anti-pyretic effect Effects 0.000 description 1
• 230000036528 appetite Effects 0.000 description 1
• 235000019789 appetite Nutrition 0.000 description 1
• 150000001805 chlorine compounds Chemical class 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• 150000002148 esters Chemical class 0.000 description 1
• 125000001033 ether group Chemical group 0.000 description 1
• OHZZTXYKLXZFSZ-UHFFFAOYSA-I manganese(3+) 5,10,15-tris(1-methylpyridin-1-ium-4-yl)-20-(1-methylpyridin-4-ylidene)porphyrin-22-ide pentachloride Chemical compound [Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Mn+3].C1=CN(C)C=CC1=C1C(C=C2)=NC2=C(C=2C=C[N+](C)=CC=2)C([N-]2)=CC=C2C(C=2C=C[N+](C)=CC=2)=C(C=C2)N=C2C(C=2C=C[N+](C)=CC=2)=C2N=C1C=C2 OHZZTXYKLXZFSZ-UHFFFAOYSA-I 0.000 description 1
• 239000000155 melt Substances 0.000 description 1
• 239000003960 organic solvent Substances 0.000 description 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
• SUSQOBVLVYHIEX-UHFFFAOYSA-N phenylacetonitrile Chemical compound N#CCC1=CC=CC=C1 SUSQOBVLVYHIEX-UHFFFAOYSA-N 0.000 description 1
• 230000006207 propylation Effects 0.000 description 1
• 238000007127 saponification reaction Methods 0.000 description 1
• 229940125723 sedative agent Drugs 0.000 description 1
• 239000000932 sedative agent Substances 0.000 description 1
• 210000002784 stomach Anatomy 0.000 description 1
• 230000009967 tasteless effect Effects 0.000 description 1
• 230000001225 therapeutic effect Effects 0.000 description 1
• 150000003672 ureas Chemical class 0.000 description 1