BE423572A - - Google Patents

Info

Publication number

BE423572A

BE423572A BE423572DA BE423572A BE 423572 A BE423572 A BE 423572A BE 423572D A BE423572D A BE 423572DA BE 423572 A BE423572 A BE 423572A

Authority

BE

Belgium

Prior art keywords

fatty

amides

grs

ether

reacted

Prior art date

Links

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• 150000001408 amides Chemical class 0.000 claims description 5
• 238000004519 manufacturing process Methods 0.000 claims description 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 10
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
• 235000011121 sodium hydroxide Nutrition 0.000 description 4
• 239000000975 dye Substances 0.000 description 2
• 238000010438 heat treatment Methods 0.000 description 2
• 238000000034 method Methods 0.000 description 2
• QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
• FXEIVSYQEOJLBU-UHFFFAOYSA-N 1-$l^{1}-selanylethanimine Chemical compound CC([Se])=N FXEIVSYQEOJLBU-UHFFFAOYSA-N 0.000 description 1
• KMTWSJDKGKRNIP-UHFFFAOYSA-N 2-methyl-2,3,3a,4,5,6-hexahydro-1,3-benzothiazole Chemical compound CC1SC=2C(N1)CCCC2 KMTWSJDKGKRNIP-UHFFFAOYSA-N 0.000 description 1
• QMSRULANFPSLDY-UHFFFAOYSA-N CC1[Se]C=2C(N1)CCCC2 Chemical compound CC1[Se]C=2C(N1)CCCC2 QMSRULANFPSLDY-UHFFFAOYSA-N 0.000 description 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
• BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical group [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
• 239000003929 acidic solution Substances 0.000 description 1
• 125000000217 alkyl group Chemical group 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 239000003085 diluting agent Substances 0.000 description 1
• 238000004821 distillation Methods 0.000 description 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
• 239000000284 extract Substances 0.000 description 1
• 125000000623 heterocyclic group Chemical group 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
• 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
• 229910052711 selenium Chemical group 0.000 description 1
• 239000011669 selenium Chemical group 0.000 description 1
• 239000000243 solution Substances 0.000 description 1
• 239000007858 starting material Substances 0.000 description 1
• 229910052717 sulfur Inorganic materials 0.000 description 1
• 239000011593 sulfur Substances 0.000 description 1
• YUKQRDCYNOVPGJ-UHFFFAOYSA-N thioacetamide Chemical compound CC(N)=S YUKQRDCYNOVPGJ-UHFFFAOYSA-N 0.000 description 1
• DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 1