GB1268240A - Formation of photographic colour images by colour coupler diffusion-transer - Google Patents
Formation of photographic colour images by colour coupler diffusion-transerInfo
- Publication number
- GB1268240A GB1268240A GB50114/69A GB5011469A GB1268240A GB 1268240 A GB1268240 A GB 1268240A GB 50114/69 A GB50114/69 A GB 50114/69A GB 5011469 A GB5011469 A GB 5011469A GB 1268240 A GB1268240 A GB 1268240A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- ethyl
- distilling
- methyl
- phenyl
- 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
- 230000015572 biosynthetic process Effects 0.000 title 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 abstract 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 3
- 238000010438 heat treatment Methods 0.000 abstract 3
- VOCILNVWSWTHNE-UHFFFAOYSA-N 1-butoxy-2-nitrobenzene Chemical compound CCCCOC1=CC=CC=C1[N+]([O-])=O VOCILNVWSWTHNE-UHFFFAOYSA-N 0.000 abstract 2
- IRTONKUCLPTRNS-UHFFFAOYSA-N 2-butoxyaniline Chemical compound CCCCOC1=CC=CC=C1N IRTONKUCLPTRNS-UHFFFAOYSA-N 0.000 abstract 2
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 abstract 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 2
- 238000009835 boiling Methods 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 abstract 1
- -1 2 - ethyl Chemical group 0.000 abstract 1
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 abstract 1
- UWKRLNWGMGJTKK-UHFFFAOYSA-N 3-[acetyl(octyl)amino]-2-methylpropanoic acid Chemical compound CC(C(=O)O)CN(C(C)=O)CCCCCCCC UWKRLNWGMGJTKK-UHFFFAOYSA-N 0.000 abstract 1
- FJTTYDAWYSZXGF-UHFFFAOYSA-N 5-nonyl-2-phenyl-4H-pyrazol-3-one Chemical compound C1(=CC=CC=C1)N1N=C(CC1=O)CCCCCCCCC FJTTYDAWYSZXGF-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
- WJYIASZWHGOTOU-UHFFFAOYSA-N Heptylamine Chemical compound CCCCCCCN WJYIASZWHGOTOU-UHFFFAOYSA-N 0.000 abstract 1
- HPOOFJQPQIZNDL-UHFFFAOYSA-N N-(2-ethylhexyl)-1-hydroxynaphthalene-2-carboxamide Chemical compound C(C)C(CNC(=O)C1=C(C2=CC=CC=C2C=C1)O)CCCC HPOOFJQPQIZNDL-UHFFFAOYSA-N 0.000 abstract 1
- LOUCDGGCRYFKCO-UHFFFAOYSA-N N-heptyl-1-hydroxynaphthalene-2-carboxamide Chemical compound C(CCCCCC)NC(=O)C1=C(C2=CC=CC=C2C=C1)O LOUCDGGCRYFKCO-UHFFFAOYSA-N 0.000 abstract 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 1
- 235000010724 Wisteria floribunda Nutrition 0.000 abstract 1
- DVECBJCOGJRVPX-UHFFFAOYSA-N butyryl chloride Chemical compound CCCC(Cl)=O DVECBJCOGJRVPX-UHFFFAOYSA-N 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- YGRJFGCEOYRREO-UHFFFAOYSA-N ethyl 3-oxooctanoate Chemical compound CCCCCC(=O)CC(=O)OCC YGRJFGCEOYRREO-UHFFFAOYSA-N 0.000 abstract 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 abstract 1
- QHDYIMWKSCJTIM-UHFFFAOYSA-N phenyl 1-hydroxynaphthalene-2-carboxylate Chemical compound C1=CC2=CC=CC=C2C(O)=C1C(=O)OC1=CC=CC=C1 QHDYIMWKSCJTIM-UHFFFAOYSA-N 0.000 abstract 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 abstract 1
- 229940067157 phenylhydrazine Drugs 0.000 abstract 1
- 235000019260 propionic acid Nutrition 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
-
- 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
- G03C7/3003—Materials characterised by the use of combinations of photographic compounds known as such, or by a particular location in the photographic element
-
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/08—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP43074386A JPS4832125B1 (enExample) | 1968-10-12 | 1968-10-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1268240A true GB1268240A (en) | 1972-03-22 |
Family
ID=13545665
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB50114/69A Expired GB1268240A (en) | 1968-10-12 | 1969-10-13 | Formation of photographic colour images by colour coupler diffusion-transer |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3676124A (enExample) |
| JP (1) | JPS4832125B1 (enExample) |
| DE (1) | DE1951327C3 (enExample) |
| GB (1) | GB1268240A (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3837852A (en) * | 1972-10-02 | 1974-09-24 | Gaf Corp | Color diffusion transfer process utilizing azo coupling to actuate diffusion of color providing species |
| JPS5722089B2 (enExample) * | 1973-11-13 | 1982-05-11 | ||
| US4066457A (en) * | 1974-12-10 | 1978-01-03 | Gaf Corporation | Color developer for diffusion transfer |
| US4066456A (en) * | 1974-12-10 | 1978-01-03 | Gaf Corporation | Incorporated carboxy substituted p-phenylenediamine color developer |
| JPS5666472U (enExample) * | 1979-10-26 | 1981-06-03 | ||
| US5118594A (en) * | 1989-06-16 | 1992-06-02 | Eastman Kodak Company | Photographic elements containing removable couplers |
| US5051343A (en) * | 1989-06-16 | 1991-09-24 | Eastman Kodak Company | Photographic elements containing removable couplers |
-
1968
- 1968-10-12 JP JP43074386A patent/JPS4832125B1/ja active Pending
-
1969
- 1969-10-11 DE DE1951327A patent/DE1951327C3/de not_active Expired
- 1969-10-13 GB GB50114/69A patent/GB1268240A/en not_active Expired
- 1969-10-13 US US866022A patent/US3676124A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS4832125B1 (enExample) | 1973-10-04 |
| DE1951327C3 (de) | 1973-10-18 |
| US3676124A (en) | 1972-07-11 |
| DE1951327A1 (de) | 1970-05-06 |
| DE1951327B2 (de) | 1973-03-29 |
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