US2964402A - Mono-acetyl indazolone color couplers - Google Patents
Mono-acetyl indazolone color couplers Download PDFInfo
- Publication number
- US2964402A US2964402A US312172A US31217252A US2964402A US 2964402 A US2964402 A US 2964402A US 312172 A US312172 A US 312172A US 31217252 A US31217252 A US 31217252A US 2964402 A US2964402 A US 2964402A
- Authority
- US
- United States
- Prior art keywords
- indazolone
- color
- image
- acetyl
- photographic
- 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 - Lifetime
Links
- FAZFFSGPPHBWJG-UHFFFAOYSA-N 4-acetylindazol-3-one Chemical compound C(C)(=O)C1=C2C(N=NC2=CC=C1)=O FAZFFSGPPHBWJG-UHFFFAOYSA-N 0.000 title description 2
- -1 AMINO Chemical class 0.000 claims description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 7
- 230000008569 process Effects 0.000 claims description 7
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- LOCAIGRSOJUCTB-UHFFFAOYSA-N indazol-3-one Chemical compound C1=CC=C2C(=O)N=NC2=C1 LOCAIGRSOJUCTB-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 229910052709 silver Inorganic materials 0.000 description 5
- 239000004332 silver Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 150000003855 acyl compounds Chemical class 0.000 description 2
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 150000008049 diazo compounds Chemical class 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical class C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- 125000004080 3-carboxypropanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C(O[H])=O 0.000 description 1
- PURJQQVODLKYOK-UHFFFAOYSA-N 4,5-diacetylindazol-3-one Chemical class C(C)(=O)C=1C(=C2C(N=NC2=CC1)=O)C(C)=O PURJQQVODLKYOK-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229950011260 betanaphthol Drugs 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 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
- G03C7/3231—Couplers containing an indazolone ring
Definitions
- the present invention constitutes an improvement in and a modification of the subject matter disolos'edin Patent 2,673,801 to Jacob Joseph Jennen, dated March 30,1954.
- a colored image may be formed by developing a reducible silver salt image in the presence of a compound which couples during development with the oxidation product of'the developing agent and forms a dyestuff.
- the dyestulf deposits onto the developed silver grams.
- Z represents the non-metallic atoms required for completing a homo-, hetero, or polycyclic nucleus.
- the polycyclic nucleus completed by Z may contain at least one further NHNH-CO group to give a compound containing two pyrazolone-3 rings.
- the compound completed by Z may contain two or more nuclei as well, linked by a chemical bond or a bior polyvalent atom or a group, such as -CH Assuming that these color couplers may be represented by the following formula:
- the dyestufi formed from thesecouplers may be writ I CH: V
- Another object of this invention is to provide new photographic developers containing a color coupler.
- a further object is to provide new photographic material containing a color coupler.
- a dyestulf having the same structure as that obtained with the compounds of Patent No. 2,673,801 is obtained by developing a reducible silver salt image with a primary aromatic amino developing agent in the presence of a compound corresponding to the formula or to a tautomeric form thereof, but having the H-atom in the 1-position of the pyrazolone-3 ring substituted by an acyl group.
- the acyl group may be bound singly or doubly.
- a double acyl, for instance, succinyl, is linked to two indazolone couplers.
- the compounds according to our present invention are monoacyl indazolones.
- acyl group is split olf by the action of the oxidation product'of the developing agent.
- the color coupler according to our invention may be obtained by acylating the color coupler of Patent 2,673,801.
- an acyl group in the 1-position may be efiected with an acid anhydride or with an acid halide. It is, however, not easy to determine the position where an acyl group enters Depending on the solvent used, for instance, with benzeneor pyridine the acyl group may be driven to different positions. During the reaction, however, rearrangements may occur. The acyl group may move from the 2-position to the 1- position, as is known with respect to 2-acyl-7-nitro indazole (Ann., 451 (1927), 303). Such final change may be obtained byboilingin nitrobenzene, acetic acid, pyridine or simply by melting.
- l-acyl indazolone derivatives according to the present invention have the advantage over the indazolone couplers according to Patent 2,673,801 of being more soluble in water. This will be clear from a comparison of the examples of this patent and the present examples.
- the solubility of our present couplers may be further enhanced by introducing into the acyl group a group conferring solubility in water without enhancingthesolubility of the image dyestuif since the acyl group is split oif on development.
- the dyestuffs obtained upon color development with the color couplers according to the present invention are more stable to acid than those obtained with the known pyrazolones having a reactive methylene group.
- the present dyestuffs that contain a substituent rendering them fast to diffusion are not removable from the emulsion layer even by prolonged washing.
- Our new color couplers may be used in the developing solution or in a colloid layer, either in a light-sensitive layer or in a non-light-sensitive layer adjacent to a sensitive layer or separated therefrom by a water-permeable colloid layer.
- monoamino developing agents we mention amino phenols, amino cresols and thier halogen derivatives, and amino naphthols.
- the developing agents which we prefer to use and that give the best results in the present process are aromatic ortho and paradiamines, such as para-phenylene diamine and its substitution products.
- Example 1 5.9 gm. indazolone in 30 cc. acetic acid anhydride are refluxed for 3 hours. To this mixture ethyl alcohol is added. After evaporation to dryness in an open dish, the residue is recrystallized from alcohol (Ann., 212 (1882), 336). Melting point 111112 C. Yield 5.6 gm. 1:3-diacetyl indazolone which corresponds to the following formula:
- G OCH 2 gm. of the indazolone derivative thus prepared are dissolved in 50 cc. water and 10 cc. of an aqueous solution of sodium hydroxide N, and added to 1 liter of a mixture of; equal parts of the following solutions Gm.
- NzN-diethyl-p-phenylene diamine hydrochloride 6 Water to 500 cc.
- B Potassium carbonate 75 Potassium bromide 2.5 Water to 500 cc.
- Example 3 gm. S-octadecenyl succinyl amino indazolone which may be prepared as described in Example 1 of Patent 2,823,998 to Jacob Joseph lennen, dated February 18, 195 8, in 40 cc. acetic anhydride are boiled for minutes. The mixture is poured into water and recrystallized from alcohol. Yield 10 gm. 1:3-diacetyl-S-octadecenyl succinyl amino indazolone corresponding to the following formula:
- Process for the production of a colored photo graphic image comprising developing a reducible silver salt image in a photographic element by means of a primary aromatic amino developing agent in the presence of a color coupler having the following formula 2.
- Photographic material comprising a silver halide emulsion layer and a colloid layer adjacent to the emulsion layer, the photographic material containing a color coupler having the following formula 4.
- Process for the production of a colored photographic image comprising developing a reducible silver salt image in a photographic element by means of a primary aromatic amino developing agent in the presence of a color coupler of the group consisting of HOOC-OHr-OH-C 0-HN (INCH,
- Photographic material comprising a silver halide emulsion layer and a colloid layer adjacent to the emul- '7 sion flayer, the photographic material containing a color coupler of the group consisting of NH 5 ooc-cH c JH-c 0-HN (mom and Cxa u 1o nooc-om-crwc O-EN aHls NH 'Reterencps' Cited in the file of this patent UNITED STATES PATENTS OTHER REFERENCES Weissberger et a1.: IACS, 65 (1943), pp. 1495-99. Ben'chte, 54 (1931), p. 1116.
Description
MONO-ACETYL INDAZOLONE COLOR COUPLERS Jacob Joseph Jennen, Antwerp, and Hendrik Pieter Eerdekens, Mortsel-Antwerp, Belgium, assignors to Gevaert Photo-Producten N. Antwerp, Belgium, a Belgian company a No Drawing. Filed Sept. 29,1952, Ser. No. 312,172 Claims priority, application Great Britain Oct. 3, 19 51 I 5 Claims, CI. 96-55 This invention relates to aprocess for the production of color'photographic images by color development in the presence of a color coupler, to photographic developers to photographic materialcontaining such couplers, and to photographic images obtained by our process.
The present invention constitutes an improvement in and a modification of the subject matter disolos'edin Patent 2,673,801 to Jacob Joseph Jennen, dated March 30,1954.
' It is known that a colored image may be formed by developing a reducible silver salt image in the presence of a compound which couples during development with the oxidation product of'the developing agent and forms a dyestuff. The dyestulf deposits onto the developed silver grams.
For developing magenta dyestufi images, compounds have been used until now which contain an active methylene group, such as pyrazolones and cyanacetic'derivatives. 7' 1 Further, according to the referred to patent a reducible In these three formulae, Z represents the non-metallic atoms required for completing a homo-, hetero, or polycyclic nucleus. l
The polycyclic nucleus completed by Z may contain at least one further NHNH-CO group to give a compound containing two pyrazolone-3 rings. The compound completed by Z may contain two or more nuclei as well, linked by a chemical bond or a bior polyvalent atom or a group, such as -CH Assuming that these color couplers may be represented by the following formula:
it is believed that the coupling with the oxidation products of the developing agent occurs at the N-atom in ortho position to the OH group. This assumption is supported by the coupling reaction of a diazo compound with para-cresol and beta-naphthol, which also takes I ten as follows:
silver salt image is developed with a primary aromatic amino developing agent in the presence of a compound corresponding to the following formula:
place in ortho position to the OH group, and by the can: pling reaction of a diazo compound with 3:4-dimethy1 S-hydroxypyrazole, which probably occurs in the same manner.
The dyestufi formed from thesecouplers may be writ I CH: V
(13 CH3 which formulae are analogous to the formulae LV of Baker for 2-substituted indazole.(cfr. I. Chem. Soc. (London),1945, 267). A 1 Now we have found that compounds corresponding to the following formula: v
,o-'oo fi or a tautomeric form thereof, but having the H-atomin the 1-position of the pyrazolone-3 ring substituted by an acyl group, also couple with the oxidation product of an amino aromatic developing agent, yielding an image dyestufi which has the same structure as that obtained when a compound having no acyl substitution is coupledz It isan object of our present invention to provide fa new p o s f e Produc i n o co or p otographic images by color development.
Another object of this invention is to provide new photographic developers containing a color coupler.
A further object is to provide new photographic material containing a color coupler.
Still further objects will become apparent from the following description.
According to our invention, a dyestulf having the same structure as that obtained with the compounds of Patent No. 2,673,801 is obtained by developing a reducible silver salt image with a primary aromatic amino developing agent in the presence of a compound corresponding to the formula or to a tautomeric form thereof, but having the H-atom in the 1-position of the pyrazolone-3 ring substituted by an acyl group.
The acyl group may be bound singly or doubly. A double acyl, for instance, succinyl, is linked to two indazolone couplers. The compounds according to our present invention are monoacyl indazolones.
It is believed that the acyl group is split olf by the action of the oxidation product'of the developing agent.
The color coupler according to our invention may be obtained by acylating the color coupler of Patent 2,673,801.
As the color couplers of the aforementioned patent correspond to the following formula:
a or a a omat c fo m h r o h and a ue. u on aeratin w l b b e to ent the r fi-rzq it on s that e e a ome a e Pos l As ar a he mon acyl compounds are concerned, 1-, 2- or 3-acylderiva; t es m y be obta ned.
The introduction of an acyl group in the 1-position may be efiected with an acid anhydride or with an acid halide. It is, however, not easy to determine the position where an acyl group enters Depending on the solvent used, for instance, with benzeneor pyridine the acyl group may be driven to different positions. During the reaction, however, rearrangements may occur. The acyl group may move from the 2-position to the 1- position, as is known with respect to 2-acyl-7-nitro indazole (Ann., 451 (1927), 303). Such final change may be obtained byboilingin nitrobenzene, acetic acid, pyridine or simply by melting.
As regards the di-acyl compounds the duration of the reaction plays a great part. We are of the opinion that'by boiling with an acid anhydride for a long time, l-3-di acyl compounds are obtained, relying for support on the experience gained by Weissberger in the preparation of 2-acetyl-5-acetoxy pyrazoles (J.A.C,S., 65 (1943), 1495-99). It is advantageous to prepare first a diacyl indazolone, partial diacylation of which leads to l-acyl indazolone. I
l-acyl indazolone derivatives according to the present invention have the advantage over the indazolone couplers according to Patent 2,673,801 of being more soluble in water. This will be clear from a comparison of the examples of this patent and the present examples. The solubility of our present couplers may be further enhanced by introducing into the acyl group a group conferring solubility in water without enhancingthesolubility of the image dyestuif since the acyl group is split oif on development. 7 I 7 While the color couplers according to Patent 2,673,801 are converted into a yellow, product when getting into contact with an alkaline oxidizing medium, such as a silver-removing bath, so that to the dyestuff image formed on color development a yellow reversal image is added, which results from the oxidation of the residual color coupler in the silver-removing bath, our present color couplers yield little or no yellow residual image.
The dyestuffs obtained upon color development with the color couplers according to the present invention are more stable to acid than those obtained with the known pyrazolones having a reactive methylene group.
The present dyestuffs that contain a substituent rendering them fast to diffusion are not removable from the emulsion layer even by prolonged washing.
Our new color couplers may be used in the developing solution or in a colloid layer, either in a light-sensitive layer or in a non-light-sensitive layer adjacent to a sensitive layer or separated therefrom by a water-permeable colloid layer.
The aromatic amino compounds which may be used as developing agents in the present process include diand tri-amino aryl compounds. Out of monoamino developing agents, we mention amino phenols, amino cresols and thier halogen derivatives, and amino naphthols.
The developing agents which we prefer to use and that give the best results in the present process are aromatic ortho and paradiamines, such as para-phenylene diamine and its substitution products.
The following examples of substituted indazolones are given to illustrate the invention without limiting, however, the scope thereof.
Example 1 5.9 gm. indazolone in 30 cc. acetic acid anhydride are refluxed for 3 hours. To this mixture ethyl alcohol is added. After evaporation to dryness in an open dish, the residue is recrystallized from alcohol (Ann., 212 (1882), 336). Melting point 111112 C. Yield 5.6 gm. 1:3-diacetyl indazolone which corresponds to the following formula:
According to Ann., 212 (1882), 336, 1-2-diacetyl indazolone is obtained, but we are of the opinion that the formula just given is correct.
2 gm. of the 1:3-diacetyl indazolone in 800 cc. water are heated for 4 hours on a boiling water bath. The mixture is filtered and the filtrate is cooled in ice (Ben, 57 (1924), 1722). Yield 1 gm. fine needles of l-acetylindazolone. Melting point 211 C. and having the following formula:
, G OCH 2 gm. of the indazolone derivative thus prepared are dissolved in 50 cc. water and 10 cc. of an aqueous solution of sodium hydroxide N, and added to 1 liter of a mixture of; equal parts of the following solutions Gm. (A) NzN-diethyl-p-phenylene diamine hydrochloride 6 Water to 500 cc. (B) Potassium carbonate 75 Potassium bromide 2.5 Water to 500 cc.
Melting point 89-90 C.
To 10 gm. of this di-acetal indazolone are added 20 cc. of an aqeous solution of NaOH N. After left to stand overnight, the mixture is filtered, and the filtrate is neutralized with a normal aqueous solution of acetic acid. The product obtained is sucked off and recrystallized from alcohol. Yield 7 gm. 1-aceta1-7-octadecenyl succinyl amino indazolone corresponding to the following formula:
Melting point l65167 C.
1 gm. of this indazolone is dissolved in 2 cc. of normal aqueous solution of potassium hydroxide, 4 cc. ethyl alcohol, and water to have a total volume of 25 cc., and is added to 100 cc. of a photographic silver halide emulsion prepared from 2.75 gm. silver nitrate. This emulsion is coated onto a support, exposed and developed with a solution obtained by mixing equal parts of the following solutions (A) N:N-diethyl-p-phenylene diamine sulphate 3.2
Sodium sulphate 5 Water to 500 cc.
(B) Potassium carbonate 75 Potassium bromide 2.5
Water to 500 cc.
After washing and further treating as usual in color development processes, a bluish-magenta image is formed.
Example 3 gm. S-octadecenyl succinyl amino indazolone which may be prepared as described in Example 1 of Patent 2,823,998 to Jacob Joseph lennen, dated February 18, 195 8, in 40 cc. acetic anhydride are boiled for minutes. The mixture is poured into water and recrystallized from alcohol. Yield 10 gm. 1:3-diacetyl-S-octadecenyl succinyl amino indazolone corresponding to the following formula:
/C--O C OCHI To 10 gm. of this di-acetyl indazolone derivative are added cc. of an aqueous solution of NaOH N. After Melting point -152 c.
6 left .to stand overnight, the'mixtureis' 'filte'red' and' tlie filtrate is neutralized with a normalaqueous s'olutionof acetic acid. The product obtained is sucked off and re= crystallized from alcohol. Yield 7 gm. l-acetyl-5-octadecenyl succinyl amino indazolone corresponding to the following formula:
( JOGHt H0 0 (k-CHr-CH-C O-BN isHea 1 gm. of this derivative added to a silver halide emulsion and developedboth as described in Example 2. A magenta-image is formed.
We claim:
1. Process for the production of a colored photo graphic image, comprising developing a reducible silver salt image in a photographic element by means of a primary aromatic amino developing agent in the presence of a color coupler having the following formula 2. Photographic developer containing a primary aromatic amino developing agent and a color coupler having the following formula O CH:
3. Photographic material comprising a silver halide emulsion layer and a colloid layer adjacent to the emulsion layer, the photographic material containing a color coupler having the following formula 4. Process for the production of a colored photographic image, comprising developing a reducible silver salt image in a photographic element by means of a primary aromatic amino developing agent in the presence of a color coupler of the group consisting of HOOC-OHr-OH-C 0-HN (INCH,
5. Photographic material comprising a silver halide emulsion layer and a colloid layer adjacent to the emul- '7 sion flayer, the photographic material containing a color coupler of the group consisting of NH 5 ooc-cH c JH-c 0-HN (mom and Cxa u 1o nooc-om-crwc O-EN aHls NH 'Reterencps' Cited in the file of this patent UNITED STATES PATENTS OTHER REFERENCES Weissberger et a1.: IACS, 65 (1943), pp. 1495-99. Ben'chte, 54 (1931), p. 1116.
Claims (1)
1. PROCESS FOR THE PRODUCTION OF A COLORED PHOTOGRAPHIC IMAGE, COMPRISING DEVELOPING A REDUCTIBLE SILVER SALT IMAGE IN A PHOTOGRAPHIC ELEMENT BY MEANS OF A PRIMARY AROMATIC AMINO DEVELOPING AGENT IN THE PRESENCE OF A COLOR COUPLER HAVING THE FOLLOWING FORMULA
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2964402X | 1951-10-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2964402A true US2964402A (en) | 1960-12-13 |
Family
ID=10918722
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US312172A Expired - Lifetime US2964402A (en) | 1951-10-03 | 1952-09-29 | Mono-acetyl indazolone color couplers |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2964402A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3133815A (en) * | 1957-03-20 | 1964-05-19 | Ici Ltd | Color photographic materials and processes |
| US3318905A (en) * | 1963-08-09 | 1967-05-09 | Acraf | 1-substituted 3-dialkylaminoalkoxy-in-dazoles and 1-substituted-3-hydroxyindazoles |
| US3486894A (en) * | 1966-03-23 | 1969-12-30 | Ferrania Spa | Color photographic images utilizing ureido indazolone couplers |
| US4481268A (en) * | 1981-02-09 | 1984-11-06 | Eastman Kodak Company | Method of forming a photographic dye image |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB599719A (en) * | 1944-12-05 | 1948-03-18 | Gen Aniline & Film Corp | Improvements in colour couplers for photographic colour development |
| GB663190A (en) * | 1948-11-23 | 1951-12-19 | Gevaert Photo Producten Naamlo | Improvements in and relating to the production of colour photographic images |
| US2872317A (en) * | 1952-03-21 | 1959-02-03 | Ici Ltd | Colour photographic images produced from indazolone colour couplers |
-
1952
- 1952-09-29 US US312172A patent/US2964402A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB599719A (en) * | 1944-12-05 | 1948-03-18 | Gen Aniline & Film Corp | Improvements in colour couplers for photographic colour development |
| GB663190A (en) * | 1948-11-23 | 1951-12-19 | Gevaert Photo Producten Naamlo | Improvements in and relating to the production of colour photographic images |
| US2872317A (en) * | 1952-03-21 | 1959-02-03 | Ici Ltd | Colour photographic images produced from indazolone colour couplers |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3133815A (en) * | 1957-03-20 | 1964-05-19 | Ici Ltd | Color photographic materials and processes |
| US3318905A (en) * | 1963-08-09 | 1967-05-09 | Acraf | 1-substituted 3-dialkylaminoalkoxy-in-dazoles and 1-substituted-3-hydroxyindazoles |
| US3486894A (en) * | 1966-03-23 | 1969-12-30 | Ferrania Spa | Color photographic images utilizing ureido indazolone couplers |
| US4481268A (en) * | 1981-02-09 | 1984-11-06 | Eastman Kodak Company | Method of forming a photographic dye image |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3061432A (en) | Pyrazolino benzimidazole color coupler | |
| US3002836A (en) | Cyan color former for color photography | |
| US3615505A (en) | Silver halide emulsion containing 2-pyrazolin-5-one color coupler | |
| US2964402A (en) | Mono-acetyl indazolone color couplers | |
| US4501898A (en) | Photographic development inhibitor (1H- or 2H-) indazolyl hydroquinone derivatives | |
| US2592363A (en) | P-phenylenediamine developer containing nu-alkylacetamido ethyl substituent | |
| US2673801A (en) | Production of color photographic images | |
| US3222176A (en) | Photographic colour images from amino substituted phenols | |
| US3337344A (en) | Color photographic silver halide emulsion | |
| US3056674A (en) | Color formers for producing yellow dye images by color development | |
| DE1282457B (en) | Color photographic recording material | |
| US2333106A (en) | Color photography | |
| US2979405A (en) | Light-sensitive photographic element containing a 1-hydroxy-2-naphthoic acid anilidecolor coupler | |
| US3892576A (en) | Photographic water-insoluble compounds having a hydrophobic diffusion-fast substituent | |
| US3294542A (en) | Photosensitive diazo compositions | |
| US3649278A (en) | Process for forming a photographic image | |
| US2500487A (en) | Yellow diffusion-fast color formers of the benzimidazole class | |
| US2395776A (en) | Color photography | |
| US2376679A (en) | Production of color photographic images | |
| US2993791A (en) | Color couplers containing long chain alkylaminoisophthalicester groups | |
| US2448939A (en) | Thioglycolic amide couplers | |
| US2547307A (en) | Yellow diffusion-fast color formers of the benzimidazole class | |
| US3619196A (en) | Light-sensitive color-photographic emulsions | |
| US2756149A (en) | Mordanting basic dyes in photography | |
| US2328652A (en) | Process of color photography and composition thereof |