SU173744A1 - - Google Patents

Info

Publication number

SU173744A1

SU173744A1 SU925258A SU925258A SU173744A1 SU 173744 A1 SU173744 A1 SU 173744A1 SU 925258 A SU925258 A SU 925258A SU 925258 A SU925258 A SU 925258A SU 173744 A1 SU173744 A1 SU 173744A1

Authority

SU

USSR - Soviet Union

Prior art keywords

acid

nitro

water

dimethylbenzophenone

aminoanthraquinone

Prior art date

Links

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• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
• 239000002253 acid Substances 0.000 description 4
• -1 4-amino-anthraquinone-2,5-dicarboxylic acid Chemical compound 0.000 description 3
• FQXWKSYELGXBRL-UHFFFAOYSA-N (2,5-dimethyl-4-nitrophenyl)-phenylmethanone Chemical compound CC1=C(C(=O)C2=CC=CC=C2)C=C(C(=C1)[N+](=O)[O-])C FQXWKSYELGXBRL-UHFFFAOYSA-N 0.000 description 2
• 239000012286 potassium permanganate Substances 0.000 description 2
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
• PJCBRWRFLHBSNH-UHFFFAOYSA-N (2,5-dimethylphenyl)-phenylmethanone Chemical compound CC1=CC=C(C)C(C(=O)C=2C=CC=CC=2)=C1 PJCBRWRFLHBSNH-UHFFFAOYSA-N 0.000 description 1
• ZYMCBJWUWHHVRX-UHFFFAOYSA-N (4-nitrophenyl)-phenylmethanone Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)C1=CC=CC=C1 ZYMCBJWUWHHVRX-UHFFFAOYSA-N 0.000 description 1
• CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
• GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
• 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 description 1
• 150000004056 anthraquinones Chemical class 0.000 description 1
• 125000001797 benzyl group Chemical class [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
• 238000006243 chemical reaction Methods 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 238000010908 decantation Methods 0.000 description 1
• 239000000706 filtrate Substances 0.000 description 1
• 229910052736 halogen Inorganic materials 0.000 description 1
• 125000001475 halogen functional group Chemical group 0.000 description 1
• 150000002367 halogens Chemical class 0.000 description 1
• 239000013067 intermediate product Substances 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 239000000203 mixture Substances 0.000 description 1
• 230000007935 neutral effect Effects 0.000 description 1
• 229910017604 nitric acid Inorganic materials 0.000 description 1
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
• 239000012044 organic layer Substances 0.000 description 1
• 239000002244 precipitate Substances 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
• 238000007127 saponification reaction Methods 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• 238000003786 synthesis reaction Methods 0.000 description 1
• 239000000984 vat dye Substances 0.000 description 1
• 238000005406 washing Methods 0.000 description 1