GB519208A - Improvements in or relating to colour photography - Google Patents

Improvements in or relating to colour photography

Info

Publication number
GB519208A
GB519208A GB2716638A GB2716638A GB519208A GB 519208 A GB519208 A GB 519208A GB 2716638 A GB2716638 A GB 2716638A GB 2716638 A GB2716638 A GB 2716638A GB 519208 A GB519208 A GB 519208A
Authority
GB
United Kingdom
Prior art keywords
groups
amino
substituted
hydroxy
atoms
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
Application number
GB2716638A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to GB2716638A priority Critical patent/GB519208A/en
Publication of GB519208A publication Critical patent/GB519208A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/32Colour coupling substances
    • G03C7/34Couplers containing phenols
    • G03C7/344Naphtholic couplers

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Cosmetics (AREA)

Abstract

519,208. 1 - Hydroxy - 2 - napthoylanhilides. KENDALL, J. D.,' and COLLINS, R. B. Sept. 17, 1938, No. 27166. Drawings to Specification. [Class 2 (iii)] [Also in Group XX] Compound of the general formula where R is a phenyl group substituted by one chlorine atom, two chlorine atoms, one bromine atom, two bromine atoms, or one chlorine atom and one bromine atom,.and where X is hydrogen, chlorine, or bromine, are prepared by condensing a 1-hydroxy-2-naphthoylhalide (which may be unsubstituted or substituted in the 4- position by a chlorine or bromine atom) with a chloraniline, dichloraniline, bromaniline, dibromaniline, or chlorbromaniline. The compounds prepared from o- and p-chlor-and bromanilines and 2:4-dichloraniline are referred to. The Provisional Specification refers to colour formers of the general formula while R1 and R2represent either the same or different atoms or groups consisting of hydrogen atoms, alky groups such as methyl, ethyl, or propyl, aryl groups such as phenyl, aralkyl groups such as benzyl, heterocyclic groups such as thiazole, thiazoline, oxazole, oxazoline, selenazole, selenazoline, pyridine, quinoline, indolenine, diazole or diazine such as pyrimidine, thiodiazole, or quinazoline, benzthiazole, naphthathiazole, and anthrathiazole, or a single cyclic grouping such as piperidine, pyrazole, indole, or N-alkyldihydrobenzthiazole and X represents hydrogen or a halogen atom. The groups R1 and R2may be substituted by halogen atoms or amino, substituted, amino, nitro, hydroxy, alkoxy, or oxyalkyl groups. The naphthalene nucleus may be substituted in any of the 3-, 5-, 6-, 7-, or 8- positions with halogen atoms or alkyl, aryl, amino, substituted amino, nitro, hydroxy, alkoxy, carbalkoxy, or oxyalkyl groups. 1-hydroxy-2-naphthoylchloride may be condensed with ammonia, aniline, monomethylaniline, p-nitroaniline, oc- or #-naphthylamine, ethyloc-naphthylamine, o- or p-anisidine, p-aminophenol, p-amino-. benzoic acid, 2:6-dibrom-4-aminophenol, maminoacetophenone, m - aminobenzaldehyde, ethyl - p -aminobenzoate, 1 - amino - 5 -ethoxybenzthiazole, 1-iminodihydrobenzthiazole, or 2-imino-1-methyl-dihydroquinoline.
GB2716638A 1938-09-17 1938-09-17 Improvements in or relating to colour photography Expired GB519208A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2716638A GB519208A (en) 1938-09-17 1938-09-17 Improvements in or relating to colour photography

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2716638A GB519208A (en) 1938-09-17 1938-09-17 Improvements in or relating to colour photography

Publications (1)

Publication Number Publication Date
GB519208A true GB519208A (en) 1940-03-19

Family

ID=10255274

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2716638A Expired GB519208A (en) 1938-09-17 1938-09-17 Improvements in or relating to colour photography

Country Status (1)

Country Link
GB (1) GB519208A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2521908A (en) * 1947-03-13 1950-09-12 Eastman Kodak Co 1-hydroxy-2-naphthamide colored couplers
US3005709A (en) * 1958-01-13 1961-10-24 Gen Aniline & Film Corp Photographic couplers containing acylamino groups
US4178183A (en) * 1978-07-27 1979-12-11 Eastman Kodak Company Thiazolyl coupler compositions and photographic elements suited to forming integral sound tracks
US4208210A (en) * 1974-12-19 1980-06-17 Fuji Photo Film Co., Ltd. Process for forming an optical soundtrack
US5030544A (en) * 1984-09-28 1991-07-09 Agfa-Gevaert, N.V. Photographic elements comprising thiazolyl couplers capable of forming infrared-absorbing dyes for integral sound track

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2521908A (en) * 1947-03-13 1950-09-12 Eastman Kodak Co 1-hydroxy-2-naphthamide colored couplers
US3005709A (en) * 1958-01-13 1961-10-24 Gen Aniline & Film Corp Photographic couplers containing acylamino groups
US4208210A (en) * 1974-12-19 1980-06-17 Fuji Photo Film Co., Ltd. Process for forming an optical soundtrack
US4178183A (en) * 1978-07-27 1979-12-11 Eastman Kodak Company Thiazolyl coupler compositions and photographic elements suited to forming integral sound tracks
US5030544A (en) * 1984-09-28 1991-07-09 Agfa-Gevaert, N.V. Photographic elements comprising thiazolyl couplers capable of forming infrared-absorbing dyes for integral sound track

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