GB675654A - Improvements in and relating to the manufacture of light-sensitive emulsions - Google Patents

Improvements in and relating to the manufacture of light-sensitive emulsions

Info

Publication number
GB675654A
GB675654A GB2770747A GB2770747A GB675654A GB 675654 A GB675654 A GB 675654A GB 2770747 A GB2770747 A GB 2770747A GB 2770747 A GB2770747 A GB 2770747A GB 675654 A GB675654 A GB 675654A
Authority
GB
United Kingdom
Prior art keywords
prepared
methyl
naphthylbenzoxazole
anilinovinyl
ethyl
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
GB2770747A
Inventor
Andre Emile Van Dormael
Leo Arnold Van De Straete
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.)
Gevaert Photo Producten NV
Original Assignee
Gevaert Photo Producten NV
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 Gevaert Photo Producten NV filed Critical Gevaert Photo Producten NV
Priority to GB2770747A priority Critical patent/GB675654A/en
Publication of GB675654A publication Critical patent/GB675654A/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
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/08Sensitivity-increasing substances
    • G03C1/10Organic substances
    • G03C1/12Methine and polymethine dyes

Landscapes

  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

41 - Methoxy - 3 - amino - 4 - hydroxydiphenyl is prepared by reducing 41-methoxy-3-nitro-4-hydroxydiphenyl with stannous chloride and HCl at boiling temperature. 2 - Methyl - 5 - p - methoxyphenylbenzoxazole is prepared by refluxing 41-methoxy-3-amino-4-hydroxydiphenyl with acetic anhydride. 2-methyl-5-b -naphthylbenzoxazole is similarly prepared. 2 - (b - ethyl : b - anilinovinyl) - 5 - p - methoxybenzoxazole dimethylsulphate is prepared by fusing 2 - methyl - 5 - p - methoxyphenylbenzoxazole dimethylsulphate with S-methyl-isothiopropionanilide. 2 - Nitro - 5 - (b - naphthyl) - phenol is prepared by nitrating p-(b -naphthyl)-phenol in acetic acid. 4-Methyl-31-nitro-41-hydroxydiphenyl is similarly prepared. 2-Amino-4-(b -naphthyl)-phenol is prepared by reducing 2 - nitro - 4 - (b - naphthyl) - phenol with stannous chloride and HCl. 4-Methyl-31-amino-4-hydroxydiphenyl is similarly prepared. 2 - b - Anilinovinyl - 5 - b - naphthylbenzoxazole benzyl bromide is prepared by fusing 2-methyl - 5 - b - naphthylbenzoxazole benzyl bromide with diphenylformamidine. 2-b -anilinovinyl - 5 - p - methoxyphenylbenzoxazole benzyl bromide is similarly prepared. 2 - Methyl - 5 - p - tolylbenzoxazole is prepared by heating 4 - methyl - 31 - amino - 41 - hydroxydiphenyl with acetyl chloride in benzene. 2 - (b - Propyl : b - anilinovinyl) - 5 - p - tolylbenzoxazole diethylsulphate is prepared by fusing 2 - methyl - 5 - p - tolylbenzoxazole diethylsulphate with ethylthiobutyrylisoanilide. 2 - Mercapto - 5 - b - naphthylbenzoxazole is prepared by refluxing 2-amino-4-b -naphthylphenol with CS2 in alcohol containing KOH. 2 - Methylmercapto - 5 - b - naphthylbenzoxazole is prepared by reacting 2-mercapto-5-b -naphthylbenzoxazole with dimethyl sulphate in alcoholic NaOH.ALSO:3 : 31 - Dimethyl - 9 - ethyl - 5 : 51 - di - p - methoxyphenyloxacarbocyanine iodide is prepared by condensing together in pyridine 2-(b -ethyl : b - anilinovinyl) - 5 - p - methoxyphenylbenzoxazole dimethylsulphate and 2-methyl-5-p-methoxyphenylbenzoxazole dimethylsulphate and treating with aqueous KI solution. 3 : 31 - Dibenzyl - 5 : 51 - di - p - methoxyphenyloxacarbocyanine bromide is prepared by reacting 2 - methyl - 5 - p - methoxyphenylbenzoxazole benzyl bromide with ethyl orthoformate in acetic anhydride. 3 - Benzyl - 31 - ethyl - 5 - b - naphthyloxathiazolinocarbocyanine iodide is prepared by condensing 2 - (b - anilinovinyl) - 5 - b - naphthylbenzoxazole benzyl bromide with 2-methylthiazoline ethyl bromide in pyridine, and treating with aqueous KI solution. 3 : 31-Dibenzyl - 41 - methyl - 5 - b - naphthyloxathiazolocarbocyanine bromide is similarly prepared. 3 : 31 - Diethyl - 9 - n - propyl - 5 : 51 - di - p - tolyloxacarbocyanine ethylsulphate is prepared by condensing 2-(b -n-propyl : b -anilinovinyl)-5-p-tolylbenzoxazole diethylsulphate and 2-methyl-5-p-tolylbenzoxazole diethylsulphate in pyridine. 11 : 3 - Diethyl - 5 - p - tolyloxa - 21 - cyanine iodide is prepared by condensing 2-methyl-5-p-tolylbenzoxazole diethylsulphate and 2-methyl-mercaptoquinoline ethyl iodide in pyridine. A hemicyanine dye is prepared by fusing together 2-methyl-5-p-tolylbenzoxazole diethylsulphate, ethyl orthoformate, and p-phenylenediamine, and converting to the iodide. A complex merocyanine dye is prepared by fusing together 5-[(1-ethylquinolylidene)-ethylidene] - 3 - allylrhodanine, 2 - methyl - 5 - p - methoxyphenylbenzoxazole, and methyl p-toluenesulphonate and converting to the iodide. 3 - Benzyl - 5 - p - methoxyphenyl - 41 - p - tolyl - 10 - acetyloxaoxodiazolocarbocyanine base is prepared by condensing 2-b -anilinovinyl-5-p-methoxyphenylbenzoxazole benzyl bromide and 2-acetylmethyl-4-p-tolyl-1 : 3 : 5-oxodiazole in acetic anhydride containing triethylamine. 5 - [(3 - Benzyl - 5 - b - naphthylbenzoxazolylidene) - ethylidene] - 3 - allylrhodanine is prepared by refluxing together 2-(b -anilinovinyl)-5-(b -naphthyl)-benzoxazole benzyl bromide, 3-allylrhodanine, acetic anhydride, and sodium acetate. 2 - p - Dimethylaminostyryl - 3 - ethyl - 5 - b - naphthylbenzoxazole ethylsulphate is prepared by boiling together 2-methyl-5-(b -naphthyl)-benzoxazole diethylsulphate and p-dimethylaminobenzaldehyde in acetic anhydride. 3 : 31 - Dibenzyl - 5 - b - naphthyl - 9 - ethoxyoxathiacarbocyanine bromide is prepared by heating together 2-(b -ethoxy : b -vinyl)-benzthiazole benzylethyl sulphate, 2 - methylmercapto - 5 - b - naphthylbenzoxazole benzyl p-toluenesulphonate, acetic anhydride, and triethylamine, and treating with aqueous KBr solution.
GB2770747A 1947-10-16 1947-10-16 Improvements in and relating to the manufacture of light-sensitive emulsions Expired GB675654A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2770747A GB675654A (en) 1947-10-16 1947-10-16 Improvements in and relating to the manufacture of light-sensitive emulsions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2770747A GB675654A (en) 1947-10-16 1947-10-16 Improvements in and relating to the manufacture of light-sensitive emulsions

Publications (1)

Publication Number Publication Date
GB675654A true GB675654A (en) 1952-07-16

Family

ID=10263988

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2770747A Expired GB675654A (en) 1947-10-16 1947-10-16 Improvements in and relating to the manufacture of light-sensitive emulsions

Country Status (1)

Country Link
GB (1) GB675654A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5422237A (en) * 1993-05-11 1995-06-06 Fuji Photo Film Co., Ltd. Methine compound and silver halide photographic material comprising the same
US5439789A (en) * 1993-05-11 1995-08-08 Fuji Photo Film Co., Ltd. Methine compound and silver halide photographic material comprising the same
US5534403A (en) * 1993-04-16 1996-07-09 Fuji Photo Film Co., Ltd. Silver halide photographic material
US5593820A (en) * 1993-12-20 1997-01-14 Fuji Photo Film Co., Ltd. Silver halide emulsion and silver halide photographic material using the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5534403A (en) * 1993-04-16 1996-07-09 Fuji Photo Film Co., Ltd. Silver halide photographic material
US5422237A (en) * 1993-05-11 1995-06-06 Fuji Photo Film Co., Ltd. Methine compound and silver halide photographic material comprising the same
US5439789A (en) * 1993-05-11 1995-08-08 Fuji Photo Film Co., Ltd. Methine compound and silver halide photographic material comprising the same
US5593820A (en) * 1993-12-20 1997-01-14 Fuji Photo Film Co., Ltd. Silver halide emulsion and silver halide photographic material using the same

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