DE239674C - - Google Patents

Info

Publication number

DE239674C

DE239674C DENDAT239674D DE239674DA DE239674C DE 239674 C DE239674 C DE 239674C DE NDAT239674 D DENDAT239674 D DE NDAT239674D DE 239674D A DE239674D A DE 239674DA DE 239674 C DE239674 C DE 239674C

Authority

DE

Germany

Prior art keywords

group

dyes

diketodihydro

class

result

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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• 239000000975 dye Substances 0.000 claims description 6
• 239000000984 vat dye Substances 0.000 claims description 2
• AUKRYONWZHRJRE-UHFFFAOYSA-N 9-anthrol Chemical compound C1=CC=C2C(O)=C(C=CC=C3)C3=CC2=C1 AUKRYONWZHRJRE-UHFFFAOYSA-N 0.000 claims 2
• YUPISCFUSYUGEY-UHFFFAOYSA-N 2-chloroindol-3-one Chemical compound C1=CC=C2C(=O)C(Cl)=NC2=C1 YUPISCFUSYUGEY-UHFFFAOYSA-N 0.000 claims 1
• 241000854350 Enicospilus group Species 0.000 claims 1
• 229910052799 carbon Inorganic materials 0.000 claims 1
• 230000005494 condensation Effects 0.000 claims 1
• 238000009833 condensation Methods 0.000 claims 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
• 125000000468 ketone group Chemical group 0.000 claims 1
• 230000008707 rearrangement Effects 0.000 claims 1
• 125000001806 thionaphthenyl group Chemical group 0.000 claims 1
• WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
• SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
• 239000000047 product Substances 0.000 description 2
• FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 239000006227 byproduct Substances 0.000 description 1
• 239000003638 chemical reducing agent Substances 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 239000000835 fiber Substances 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 230000003647 oxidation Effects 0.000 description 1
• 238000007254 oxidation reaction Methods 0.000 description 1
• 239000002244 precipitate Substances 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 238000003756 stirring Methods 0.000 description 1
• QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1