DE184808C - - Google Patents

Info

Publication number

DE184808C

DE184808C DENDAT184808D DE184808DA DE184808C DE 184808 C DE184808 C DE 184808C DE NDAT184808 D DENDAT184808 D DE NDAT184808D DE 184808D A DE184808D A DE 184808DA DE 184808 C DE184808 C DE 184808C

Authority

DE

Germany

Prior art keywords

aniline

condensation product

anthrachryson

formaldehyde

orange

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.)

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• WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 9
• 239000007859 condensation product Substances 0.000 claims description 5
• RKYAZRHUKGRDNT-UHFFFAOYSA-N heptacyclo[16.12.0.02,11.03,8.012,17.021,30.023,28]triaconta-1(18),2(11),3,5,7,12,14,16,19,21,23,25,27,29-tetradecaen-9-one Chemical compound C12=C3C=C4C=CC=CC4=CC3=CC=C2C2=CC=CC=C2C2=C1C1=CC=CC=C1C(=O)C2 RKYAZRHUKGRDNT-UHFFFAOYSA-N 0.000 claims description 4
• PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 3
• 238000000034 method Methods 0.000 claims description 3
• 239000012670 alkaline solution Substances 0.000 claims description 2
• 150000004056 anthraquinones Chemical class 0.000 claims description 2
• 238000002360 preparation method Methods 0.000 claims description 2
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
• 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• 150000003142 primary aromatic amines Chemical class 0.000 claims 1
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 17
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
• 150000001875 compounds Chemical class 0.000 description 2
• 239000013078 crystal Substances 0.000 description 2
• -1 nitrogen-containing anthraquinone Chemical class 0.000 description 2
• 239000000047 product Substances 0.000 description 2
• 239000000126 substance Substances 0.000 description 2
• CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
• 239000002253 acid Substances 0.000 description 1
• 230000002378 acidificating effect Effects 0.000 description 1
• 150000007513 acids Chemical class 0.000 description 1
• 150000001555 benzenes Chemical class 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 239000003518 caustics Substances 0.000 description 1
• 239000000975 dye Substances 0.000 description 1
• 239000000706 filtrate Substances 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 229910052500 inorganic mineral Inorganic materials 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 238000002844 melting Methods 0.000 description 1
• 230000008018 melting Effects 0.000 description 1
• WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
• 239000011707 mineral Substances 0.000 description 1
• 239000000203 mixture Substances 0.000 description 1
• 239000003960 organic solvent Substances 0.000 description 1
• 150000003141 primary amines Chemical class 0.000 description 1
• 239000000243 solution Substances 0.000 description 1
• 150000004992 toluidines Chemical class 0.000 description 1