GB662419A - Production of yellow dye photographic images by color development - Google Patents
Production of yellow dye photographic images by color developmentInfo
- Publication number
- GB662419A GB662419A GB31880/49A GB3188049A GB662419A GB 662419 A GB662419 A GB 662419A GB 31880/49 A GB31880/49 A GB 31880/49A GB 3188049 A GB3188049 A GB 3188049A GB 662419 A GB662419 A GB 662419A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- acid
- bis
- condensing
- reducing
- 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.)
- Expired
Links
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 title 1
- 239000001043 yellow dye Substances 0.000 title 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 4
- SKDHHIUENRGTHK-UHFFFAOYSA-N 4-nitrobenzoyl chloride Chemical compound [O-][N+](=O)C1=CC=C(C(Cl)=O)C=C1 SKDHHIUENRGTHK-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- -1 2 - (p - Benzoylacetamidophenyl) - 1 - octadecyl Chemical group 0.000 abstract 2
- BEWGVKVWWKCFHO-UHFFFAOYSA-N 3-(4-aminophenyl)-3-oxopropanenitrile Chemical compound NC1=CC=C(C(=O)CC#N)C=C1 BEWGVKVWWKCFHO-UHFFFAOYSA-N 0.000 abstract 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 230000000802 nitrating effect Effects 0.000 abstract 2
- 150000002828 nitro derivatives Chemical class 0.000 abstract 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 2
- 238000010992 reflux Methods 0.000 abstract 2
- 239000008096 xylene Substances 0.000 abstract 2
- GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical compound C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 abstract 1
- NOZORYFNDJDVET-UHFFFAOYSA-N 2-(7-aminonaphthalen-1-yl)oxyacetic acid Chemical compound NC1=CC=C2C=CC=C(C2=C1)OCC(=O)O NOZORYFNDJDVET-UHFFFAOYSA-N 0.000 abstract 1
- SUFSOQJBQWQPMA-UHFFFAOYSA-N 2-[8-[(3-oxo-3-phenylpropanoyl)amino]naphthalen-1-yl]oxyacetic acid Chemical compound C(C1=CC=CC=C1)(=O)CC(=O)NC=1C=CC=C2C=CC=C(C12)OCC(=O)O SUFSOQJBQWQPMA-UHFFFAOYSA-N 0.000 abstract 1
- AJHPGXZOIAYYDW-UHFFFAOYSA-N 3-(2-cyanophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound CC(C)(C)OC(=O)NC(C(O)=O)CC1=CC=CC=C1C#N AJHPGXZOIAYYDW-UHFFFAOYSA-N 0.000 abstract 1
- WJBPBFGYMVQHDE-UHFFFAOYSA-N 3-[4-(3-ethoxy-3-oxopropanoyl)phenyl]-3-oxopropanoic acid Chemical compound CCOC(=O)CC(=O)C1=CC=C(C(=O)CC(O)=O)C=C1 WJBPBFGYMVQHDE-UHFFFAOYSA-N 0.000 abstract 1
- AEWZMTVRFCTONS-UHFFFAOYSA-N 3-amino-4-(octadecylamino)benzenesulfonic acid Chemical compound CCCCCCCCCCCCCCCCCCNC1=CC=C(S(O)(=O)=O)C=C1N AEWZMTVRFCTONS-UHFFFAOYSA-N 0.000 abstract 1
- KAYAKFYASWYOEB-UHFFFAOYSA-N 3-octadec-1-enyloxolane-2,5-dione Chemical compound CCCCCCCCCCCCCCCCC=CC1CC(=O)OC1=O KAYAKFYASWYOEB-UHFFFAOYSA-N 0.000 abstract 1
- YLBNZBGHVFUFCV-UHFFFAOYSA-N 4,6-dimethoxybenzene-1,3-diol Chemical compound COC1=CC(OC)=C(O)C=C1O YLBNZBGHVFUFCV-UHFFFAOYSA-N 0.000 abstract 1
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 abstract 1
- GKKZMYDNDDMXSE-UHFFFAOYSA-N Ethyl 3-oxo-3-phenylpropanoate Chemical compound CCOC(=O)CC(=O)C1=CC=CC=C1 GKKZMYDNDDMXSE-UHFFFAOYSA-N 0.000 abstract 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 1
- MKXQLKNBJKSNHP-UHFFFAOYSA-N [3-[(4-aminobenzoyl)amino]-5-(octadecanoylamino)phenyl]methanesulfonic acid Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC=1C=C(CS(=O)(=O)O)C=C(C=1)NC(C1=CC=C(C=C1)N)=O MKXQLKNBJKSNHP-UHFFFAOYSA-N 0.000 abstract 1
- QTXAQOYWYDYTHQ-UHFFFAOYSA-N [3-[(4-nitrobenzoyl)amino]-5-(octadecanoylamino)phenyl]methanesulfonic acid Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC=1C=C(CS(=O)(=O)O)C=C(C=1)NC(C1=CC=C(C=C1)[N+](=O)[O-])=O QTXAQOYWYDYTHQ-UHFFFAOYSA-N 0.000 abstract 1
- PQZWOOQNPBEUOV-UHFFFAOYSA-N [3-amino-5-(octadecanoylamino)phenyl]methanesulfonic acid Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)NC=1C=C(CS(=O)(=O)O)C=C(C=1)N PQZWOOQNPBEUOV-UHFFFAOYSA-N 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 abstract 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 abstract 1
- 125000005594 diketone group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- TVEJCFVSJDAOMZ-UHFFFAOYSA-N n-(8-hydroxynaphthalen-2-yl)acetamide Chemical compound C1=CC=C(O)C2=CC(NC(=O)C)=CC=C21 TVEJCFVSJDAOMZ-UHFFFAOYSA-N 0.000 abstract 1
- CHLCPTJLUJHDBO-UHFFFAOYSA-M sodium;benzenesulfinate Chemical compound [Na+].[O-]S(=O)C1=CC=CC=C1 CHLCPTJLUJHDBO-UHFFFAOYSA-M 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/3244—Couplers forming azinic dyes; Specific developers therefor
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US66825A US2522802A (en) | 1948-12-22 | 1948-12-22 | Production of yellow dye images by color development |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB662419A true GB662419A (en) | 1951-12-05 |
Family
ID=22071952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB31880/49A Expired GB662419A (en) | 1948-12-22 | 1949-12-12 | Production of yellow dye photographic images by color development |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2522802A (enrdf_load_stackoverflow) |
| BE (1) | BE492847A (enrdf_load_stackoverflow) |
| CH (1) | CH289721A (enrdf_load_stackoverflow) |
| DE (1) | DE827901C (enrdf_load_stackoverflow) |
| FR (1) | FR1003992A (enrdf_load_stackoverflow) |
| GB (1) | GB662419A (enrdf_load_stackoverflow) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3099559A (en) * | 1959-08-31 | 1963-07-30 | Gen Aniline & Film Corp | Silver-free color reproduction process and composition therefor |
| BE584330A (enrdf_load_stackoverflow) * | 1959-11-05 | |||
| US4066456A (en) * | 1974-12-10 | 1978-01-03 | Gaf Corporation | Incorporated carboxy substituted p-phenylenediamine color developer |
| US4066457A (en) * | 1974-12-10 | 1978-01-03 | Gaf Corporation | Color developer for diffusion transfer |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE465025A (enrdf_load_stackoverflow) * | 1945-01-27 |
-
0
- BE BE492847D patent/BE492847A/xx unknown
-
1948
- 1948-12-22 US US66825A patent/US2522802A/en not_active Expired - Lifetime
-
1949
- 1949-12-12 GB GB31880/49A patent/GB662419A/en not_active Expired
- 1949-12-16 DE DEG607A patent/DE827901C/de not_active Expired
- 1949-12-20 FR FR1003992D patent/FR1003992A/fr not_active Expired
- 1949-12-22 CH CH289721D patent/CH289721A/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH289721A (fr) | 1953-03-31 |
| US2522802A (en) | 1950-09-19 |
| BE492847A (enrdf_load_stackoverflow) | |
| DE827901C (de) | 1952-03-17 |
| FR1003992A (fr) | 1952-03-24 |
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