GB714012A - Photographic colour correction processes - Google Patents
Photographic colour correction processesInfo
- Publication number
- GB714012A GB714012A GB18680/52A GB1868052A GB714012A GB 714012 A GB714012 A GB 714012A GB 18680/52 A GB18680/52 A GB 18680/52A GB 1868052 A GB1868052 A GB 1868052A GB 714012 A GB714012 A GB 714012A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzaldehyde
- ethylene glycol
- group
- prepared
- carbo
- 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
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
- G03C7/18—Processes for the correction of the colour image in subtractive colour photography
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The polyvinyl acetal of 3-(carbo-p-cresoxyamino)-benzaldehyde, containing methylidenephenyl-o-sulphonate groups for increased solubility, is prepared by adding phosphoric acid to a solution of polyvinyl alcohol and sodium benzaldehyde-o-sulphonate in ethylene glycol and stirring, adding a dioxane solution of 3-(carbo-p-cresoxyamino)-benzaldehyde ethylene glycol acetal thereto and stirring, adding a methanol solution of triethylamine to neutralize the phosphoric acid, and precipitating with acetone. The polyvinyl acetal of 3-aminobenzaldehyde containing sodium methylidene phenyl-o-sulphonate is prepared either by hydrolyzing an aqueous ethanol solution of the above polyvinyl acetal with aqueous sodium hydroxide solution, or by stirring a mixture of polyvinyl alcohol, sodium benzaldehyde-o-sulphonate, ethylene glycol, phosphoric acid, and phosphoric anhydride, adding an ethylene glycol solution of m-aminobenzaldehyde ethylene glycol acetal and continuing stirring, and isolating as before. The polyvinyl acetals of 3-(carbo-p-cresoxyamino)-4-methoxybenzaldehyde, of 3-amino-4-methoxybenzaldehyde, of m-(5-carbethoxyamino-2-chlorobenzamido)-benzaldehyde, of m-(5-carbo-methoxyamino - 2 - chlorobenzamido) - benzaldehyde, of m-(5-carbo-p-cresoxyamino-2-chlorobenzamido)-benzaldehyde, and of m-(5-amino-2-chlorobenzamido)-benzaldehyde, all containing methylidenephenyl-o-sulphonate groups, are similarly prepared. Specifications 458,400, [Group XX], 469,108, 598,477, 600,023, 602,881, [Group XX], 627,125, 631,269, [Group IV (b)], 635,294, 638,895, 641,368, [Group XX], 652,928, and 662,793 are referred to.ALSO:3 - Nitro - 5 - stearamidobenzoic acid is prepared by heating together 3-nitro-5-aminobenzoic acid, stearoyl chloride, and pyridine. 3 - Amino - 5 - stearamidobenzoic acid is prepared by reducing 3-nitro-5-stearamidobenzoic acid in ethanol with hydrogen under pressure in the presence of palladium - on - charcoal catalyst. 3 - (Carbo - p - cresoxyamino) - benzaldehyde ethylene glycol acetal is prepared by adding p-cresyl chloroformate to a mixture of an acetone solution of m-aminobenzaldehyde ethylene glycol acetal and aqueous sodium carbonate. 3 - (Carbo - p - cresoxyamino) - 4 - methoxy - benzaldehyde ethylene glycol acetal is similarly prepared. M - (5 - Carbethoxyamino - 2 - chlorobenzamido)-benzaldehyde ethylene glycol acetal is prepared by adding a dioxane solution of 5-carbethoxyamino-2-chlorobenzoyl chloride to a mixture of a dioxane solution of m-aminobenzaldehyde ethylene glycol acetal and aqueous sodium carbonate. M-(5-Carbomethoxyamino - 2 - chlorobenzamido) - and m - (5-carbo - p - cresoxyamino - 2 - chlorobenzamido)-ethylene glycol acetals are similarly prepared. 5 - Carbethoxyamino - 2 - chlorobenzoyl chloride is obtained by reacting 5-carbethoxyamino-2-chlorobenzoic acid with thionyl chloride. 5 - Carbethoxyamino - 2 - chlorobenzoic acid is prepared by adding ethyl chloroformate to an aqueous solution of 2-chloro-5-aminobenzoic acid containing sodium carbonate. Specifications 458,400, [Group XX], 469,108, 598,477, 600,023, [Group IV (a)], 602,881, [Group XX], 627,125, 631,269, 635,294, 638,895, 641,368, [Group XX], 652,928, and 662,793, [Group IV (a)], are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US238384A US2697662A (en) | 1951-07-24 | 1951-07-24 | Color correction processes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB714012A true GB714012A (en) | 1954-08-18 |
Family
ID=22897646
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB18680/52A Expired GB714012A (en) | 1951-07-24 | 1952-07-23 | Photographic colour correction processes |
Country Status (2)
Country | Link |
---|---|
US (1) | US2697662A (en) |
GB (1) | GB714012A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE567154A (en) * | 1957-04-26 | |||
DE1142757B (en) * | 1961-03-14 | 1963-01-24 | Agfa Ag | Process for improving color reproduction when reproducing multicolor images with the aid of two color masks |
US4680356A (en) * | 1985-01-02 | 1987-07-14 | Eastman Kodak Company | Colorless ligand-releasing monomers and polymers and their use to provide dyes with metal ions |
US4557998A (en) * | 1985-01-02 | 1985-12-10 | Eastman Kodak Company | Colorless ligand-releasing monomers and polymers and their use to provide dyes with metal ions |
EP2423188B1 (en) * | 2003-08-29 | 2021-03-10 | Mitsui Chemicals Agro, Inc. | Intermediates in the preparation of agricultural/horticultural insecticides and method for using the same |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2306410A (en) * | 1936-07-07 | 1942-12-29 | Eastman Kodak Co | Color development |
GB503824A (en) * | 1936-07-07 | 1939-04-11 | Kodak Ltd | Process of colour photography |
US2328034A (en) * | 1940-12-14 | 1943-08-31 | Du Pont | Photographic element and process |
BE476358A (en) * | 1944-05-03 |
-
1951
- 1951-07-24 US US238384A patent/US2697662A/en not_active Expired - Lifetime
-
1952
- 1952-07-23 GB GB18680/52A patent/GB714012A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US2697662A (en) | 1954-12-21 |
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