AT47527B - Process for the preparation of vat-coloring anthraquinonimides. - Google Patents
Process for the preparation of vat-coloring anthraquinonimides.Info
- Publication number
- AT47527B AT47527B AT47527DA AT47527B AT 47527 B AT47527 B AT 47527B AT 47527D A AT47527D A AT 47527DA AT 47527 B AT47527 B AT 47527B
- Authority
- AT
- Austria
- Prior art keywords
- sep
- vat
- anthraquinonimides
- coloring
- preparation
- Prior art date
Links
- 238000004040 coloring Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- FPKCTSIVDAWGFA-UHFFFAOYSA-N 2-chloroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3C(=O)C2=C1 FPKCTSIVDAWGFA-UHFFFAOYSA-N 0.000 description 3
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 2
- BOCJQSFSGAZAPQ-UHFFFAOYSA-N 1-chloroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2Cl BOCJQSFSGAZAPQ-UHFFFAOYSA-N 0.000 description 2
- XOGPDSATLSAZEK-UHFFFAOYSA-N 2-Aminoanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(N)=CC=C3C(=O)C2=C1 XOGPDSATLSAZEK-UHFFFAOYSA-N 0.000 description 2
- 240000007817 Olea europaea Species 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- LRZQPQJEYDUCKH-UHFFFAOYSA-N n-(6-chloro-9,10-dioxoanthracen-1-yl)benzamide Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3C(=O)C2=C1NC(=O)C1=CC=CC=C1 LRZQPQJEYDUCKH-UHFFFAOYSA-N 0.000 description 2
- VYIDDNKEDYNTDG-UHFFFAOYSA-N n-(7-chloro-9,10-dioxoanthracen-1-yl)benzamide Chemical compound C=12C(=O)C3=CC(Cl)=CC=C3C(=O)C2=CC=CC=1NC(=O)C1=CC=CC=C1 VYIDDNKEDYNTDG-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
- 244000061775 Olea africana Species 0.000 description 1
- 235000002852 Olea africana Nutrition 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical group C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- FNCVZYRPXOZNSM-UHFFFAOYSA-N n-(4-chloro-9,10-dioxoanthracen-1-yl)benzamide Chemical compound C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(Cl)=CC=C1NC(=O)C1=CC=CC=C1 FNCVZYRPXOZNSM-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
EMI1.1
EMI1.2
EMI1.3
<tb>
<tb> ,. <SEP>
<tb>
' <SEP> ¯ <SEP> Losune <SEP> im <SEP> Pyridin <SEP> Lösung <SEP> in <SEP> Farbung <SEP> auf <SEP> Raum
<tb> Farbstoff <SEP> aus <SEP> (Chinolin) <SEP> konzentriertst <SEP> wolls
<tb> Schwefelsaure
<tb> 1-Benzoylamino-4-aminoauthrachinon <SEP> + <SEP> 2-Chloranthrachinon <SEP> oder <SEP> 1-Benzoylamino-4-Chloranthrachinon <SEP> . <SEP> 2-Aminoanthrachinon <SEP> . <SEP> braunviolett <SEP> braunolive <SEP> brau@@@@@
<tb> 1-Benzoylamino <SEP> 4 <SEP> chloranthrachinon <SEP> - <SEP> 1-Aminoauthrachinon...... <SEP> violettrot <SEP> grün <SEP> stumpfviolett
<tb> Ii
<tb> 1-Benzoylamino-5-aminoshthrachinon <SEP> - <SEP> 2-Chloranthrachinon........ <SEP> oraugerot <SEP> grüngran <SEP> kupferrot
<tb> 1-Benzoylamino-6-chloranthrachinon <SEP> Gemisch
<tb> 1-Benzoylamino-7-chloranthrachinon
<tb> 4 <SEP> 1-Aminoanthrachinon <SEP> .. <SEP> ...
<SEP> orange <SEP> blau <SEP> orangerot
<tb> 1-Henzoylamino-4-chlorantrachinon <SEP> # <SEP> 1#5-di- <SEP> dhalte <SEP> Kupe <SEP> grauviolett
<tb> aminoanthrachinon <SEP> ............. <SEP> violett) <SEP> olive <SEP> warme <SEP> küpe <SEP> violettgrau
<tb> Dibenzoyl <SEP> 1 <SEP> 5-diamino <SEP> 4#8-diaminoanthrachinon-
<tb> 2-Chloranthrachinon <SEP> ..... <SEP> blaugr#n) <SEP> blau <SEP> graugrün
<tb> Dihenzoyl-1-5-diamino-4 <SEP> chloranthrachinon <SEP> @
<tb> - <SEP> 2-Aminoanthrachinon <SEP> .....
<SEP> braun <SEP> olive <SEP> brann
<tb>
<Desc/Clms Page number 2>
EMI2.1
EMI2.2
<tb>
<tb> @ <SEP> Aussehen <SEP> Lösung <SEP> in <SEP> Pyridin <SEP> Lösung <SEP> in
<tb> konzentrierter
<tb> Schwefelsäure
<tb> 1-Benzoylamino-6-chloranthrachinon <SEP> Gemisch <SEP> gelbes
<tb> 1-Benzoylamino-7-chloranthrachinon <SEP> Kristallmehl
<tb> 1#5 <SEP> Dibenzoyldiamino-4#8-diaminoanthrachinon <SEP> .. <SEP> dunkelviolette
<tb> Nadeln <SEP> blau <SEP> gelb
<tb> braunrote
<tb> Prismen <SEP> mit
<tb> 1#5-Dibenzoyldiamino-4-chloranthrachinon.... <SEP> grüuem <SEP> goldgelb <SEP> brannolive
<tb> Schimmer
<tb>
<Desc / Clms Page number 1>
EMI1.1
EMI1.2
EMI1.3
<tb>
<tb>,. <SEP>
<tb>
'<SEP> ¯ <SEP> Losune <SEP> in <SEP> pyridine <SEP> solution <SEP> in <SEP> color <SEP> on <SEP> space
<tb> Dye <SEP> from <SEP> (quinoline) <SEP> concentrated <SEP> wolls
<tb> sulfuric acid
<tb> 1-Benzoylamino-4-aminoauthraquinone <SEP> + <SEP> 2-chloroanthraquinone <SEP> or <SEP> 1-benzoylamino-4-chloroanthraquinone <SEP>. <SEP> 2-aminoanthraquinone <SEP>. <SEP> brown violet <SEP> brown olive <SEP> brown @@@@@
<tb> 1-Benzoylamino <SEP> 4 <SEP> chloranthraquinone <SEP> - <SEP> 1-aminoauthraquinone ...... <SEP> violet-red <SEP> green <SEP> dull violet
<tb> II
<tb> 1-Benzoylamino-5-aminoshthraquinone <SEP> - <SEP> 2-chloroanthraquinone ........ <SEP> orange red <SEP> green-gray <SEP> copper-red
<tb> 1-Benzoylamino-6-chloroanthraquinone <SEP> mixture
<tb> 1-Benzoylamino-7-chloroanthraquinone
<tb> 4 <SEP> 1-aminoanthraquinone <SEP> .. <SEP> ...
<SEP> orange <SEP> blue <SEP> orange-red
<tb> 1-Henzoylamino-4-chlorantraquinone <SEP> # <SEP> 1 # 5-di- <SEP> d keep <SEP> cup <SEP> gray-violet
<tb> aminoanthraquinone <SEP> ............. <SEP> violet) <SEP> olive <SEP> warm <SEP> vat <SEP> violet-gray
<tb> Dibenzoyl <SEP> 1 <SEP> 5-diamino <SEP> 4 # 8-diaminoanthraquinone-
<tb> 2-chloroanthraquinone <SEP> ..... <SEP> blue-green # n) <SEP> blue <SEP> gray-green
<tb> Dihenzoyl-1-5-diamino-4 <SEP> chloranthraquinone <SEP> @
<tb> - <SEP> 2-aminoanthraquinone <SEP> .....
<SEP> brown <SEP> olive <SEP> burnt
<tb>
<Desc / Clms Page number 2>
EMI2.1
EMI2.2
<tb>
<tb> @ <SEP> Appearance <SEP> solution <SEP> in <SEP> pyridine <SEP> solution <SEP> in
<tb> more concentrated
<tb> sulfuric acid
<tb> 1-Benzoylamino-6-chloroanthraquinone <SEP> mixture <SEP> yellow
<tb> 1-Benzoylamino-7-chloranthraquinone <SEP> crystal flour
<tb> 1 # 5 <SEP> dibenzoyldiamino-4 # 8-diaminoanthraquinone <SEP> .. <SEP> dark purple
<tb> needles <SEP> blue <SEP> yellow
<tb> brownish red
<tb> prisms <SEP> with
<tb> 1 # 5-Dibenzoyldiamino-4-chloroanthraquinone .... <SEP> green <SEP> golden yellow <SEP> brannolive
<tb> shimmer
<tb>
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE47527X | 1909-04-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT47527B true AT47527B (en) | 1911-04-25 |
Family
ID=5625671
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT47527D AT47527B (en) | 1909-04-16 | 1910-04-09 | Process for the preparation of vat-coloring anthraquinonimides. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT47527B (en) |
-
1910
- 1910-04-09 AT AT47527D patent/AT47527B/en active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AT47527B (en) | Process for the preparation of vat-coloring anthraquinonimides. | |
| US1841369A (en) | Educational and amusement device | |
| AT48243B (en) | Process for the preparation of vat dyes of the anthracene series. | |
| AT49485B (en) | Process for the preparation of vat-coloring arylaminoanthraquinones. | |
| AT45026B (en) | Process for the preparation of acidic wool dyes of the anthracene series. | |
| AT41478B (en) | Process for the preparation of vat dyes of the anthracene series. | |
| AT33991B (en) | Process for the preparation of nitrogen-containing anthraquinone derivatives. | |
| AT43885B (en) | Process for the preparation of the benzoylaminoanthraquinone derivatives which can be used as vat dyes. | |
| AT50291B (en) | Process for the preparation of nitrogen-containing anthraquinone derivatives. | |
| AT35430B (en) | Process for the preparation of nitrogen-containing anthracene derivatives. | |
| DE633353C (en) | Process for the preparation of compounds of the chrysenequinone series | |
| AT40170B (en) | Process for the preparation of nitrogen-containing anthraquinone derivatives. | |
| DE486439C (en) | Process for the manufacture of related azo dyes | |
| DE230409C (en) | ||
| AT43726B (en) | Process for producing true colorations on the unstained vegetable fiber. | |
| AT138732B (en) | Procedure for making the glasses colored with the rare earth oxides red. | |
| AT131101B (en) | Process for the representation of insoluble azo dyes on the fiber. | |
| AT141859B (en) | Process for dyeing leather. | |
| DIX | Occurrence of Blue Constituent in High-strength Manganese Bronze | |
| AT49190B (en) | Process for the preparation of acidic wool dyes. | |
| GB440481A (en) | Colouring sands | |
| GB468686A (en) | Improvements in the manufacture and production of vat dyestuffs of the anthraquinone series | |
| DE485522C (en) | Process for the preparation of Kuepen dyes | |
| DE637939C (en) | Process for the preparation of dyes of the triarylmethane series | |
| DE514973C (en) | Process for the preparation of azophthalein dyes |