DE254450C - - Google Patents

Info

Publication number

DE254450C

DE254450C DENDAT254450D DE254450DA DE254450C DE 254450 C DE254450 C DE 254450C DE NDAT254450 D DENDAT254450 D DE NDAT254450D DE 254450D A DE254450D A DE 254450DA DE 254450 C DE254450 C DE 254450C

Authority

DE

Germany

Prior art keywords

nitroanthraquinones

ligroin

chlorine

nitro

parts

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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• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
• 239000000460 chlorine Substances 0.000 claims description 5
• 229910052801 chlorine Inorganic materials 0.000 claims description 5
• 239000002904 solvent Substances 0.000 claims description 3
• 238000000034 method Methods 0.000 claims description 2
• 230000004048 modification Effects 0.000 claims 1
• 238000012986 modification Methods 0.000 claims 1
• 239000000375 suspending agent Substances 0.000 claims 1
• RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 3
• 238000002844 melting Methods 0.000 description 3
• 230000008018 melting Effects 0.000 description 3
• 239000000203 mixture Substances 0.000 description 3
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
• QWVMIYZXMZSUIZ-UHFFFAOYSA-N 2-methyl-3-nitroanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=C(C)C([N+]([O-])=O)=C2 QWVMIYZXMZSUIZ-UHFFFAOYSA-N 0.000 description 2
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
• 238000009835 boiling Methods 0.000 description 2
• 238000005660 chlorination reaction Methods 0.000 description 2
• 239000000725 suspension Substances 0.000 description 2
• YQZHOBBQNFBTJE-UHFFFAOYSA-N 2-chloro-3-methylanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=C(C)C(Cl)=C2 YQZHOBBQNFBTJE-UHFFFAOYSA-N 0.000 description 1
• XPVWLINABRAODC-UHFFFAOYSA-N 3-chloro-9,10-dioxoanthracene-2-carbaldehyde Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=C(Cl)C(C=O)=C2 XPVWLINABRAODC-UHFFFAOYSA-N 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
• 229960000583 acetic acid Drugs 0.000 description 1
• WLJVXDMOQOGPHL-UHFFFAOYSA-N benzyl-alpha-carboxylic acid Natural products OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• SNOLCJGSEPTCMD-UHFFFAOYSA-N ethyl 5-methyl-1,3-thiazole-4-carboxylate Chemical compound CCOC(=O)C=1N=CSC=1C SNOLCJGSEPTCMD-UHFFFAOYSA-N 0.000 description 1
• 239000012362 glacial acetic acid Substances 0.000 description 1
• 229960003424 phenylacetic acid Drugs 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 239000011541 reaction mixture Substances 0.000 description 1
• 229910000029 sodium carbonate Inorganic materials 0.000 description 1
• 239000007787 solid Substances 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1

Cited By (2)