GB1356175A - Colour photogrphic silver halide material - Google Patents
Colour photogrphic silver halide materialInfo
- Publication number
- GB1356175A GB1356175A GB3693071A GB3693071A GB1356175A GB 1356175 A GB1356175 A GB 1356175A GB 3693071 A GB3693071 A GB 3693071A GB 3693071 A GB3693071 A GB 3693071A GB 1356175 A GB1356175 A GB 1356175A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dicyclopentyl
- prepared
- methylphenoxy
- acid
- refluxing
- 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
- -1 silver halide Chemical class 0.000 title abstract 4
- 239000000463 material Substances 0.000 title 1
- 229910052709 silver Inorganic materials 0.000 title 1
- 239000004332 silver Substances 0.000 title 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 6
- 238000010992 reflux Methods 0.000 abstract 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- GOXKGNBQJTYZSE-UHFFFAOYSA-N 2,5-dicyclopentyl-4-methylphenol Chemical compound OC=1C=C(C2CCCC2)C(C)=CC=1C1CCCC1 GOXKGNBQJTYZSE-UHFFFAOYSA-N 0.000 abstract 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 235000019441 ethanol Nutrition 0.000 abstract 3
- 238000010438 heat treatment Methods 0.000 abstract 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 abstract 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 abstract 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004494 ethyl ester group Chemical group 0.000 abstract 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- 239000008096 xylene Substances 0.000 abstract 2
- ATDJTYYAKXLKSY-UHFFFAOYSA-N 2,4-dicyclopentyl-5-methylphenol Chemical compound CC1=CC(O)=C(C2CCCC2)C=C1C1CCCC1 ATDJTYYAKXLKSY-UHFFFAOYSA-N 0.000 abstract 1
- NVJPXDFLCUBKCF-UHFFFAOYSA-N 2-(2,5-dicyclopentyl-4-methylphenoxy)propanoic acid Chemical compound C1(CCCC1)C1=C(OC(C(=O)O)C)C=C(C(=C1)C)C1CCCC1 NVJPXDFLCUBKCF-UHFFFAOYSA-N 0.000 abstract 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- OBIBGKIPVHTJDD-UHFFFAOYSA-N 4-(2,5-dicyclopentyl-4-methylphenoxy)butanenitrile Chemical compound C1(CCCC1)C1=C(OCCCC#N)C=C(C(=C1)C)C1CCCC1 OBIBGKIPVHTJDD-UHFFFAOYSA-N 0.000 abstract 1
- ZFCFBWSVQWGOJJ-UHFFFAOYSA-N 4-chlorobutanenitrile Chemical compound ClCCCC#N ZFCFBWSVQWGOJJ-UHFFFAOYSA-N 0.000 abstract 1
- ZOQYQHLEDJOHOK-UHFFFAOYSA-N 6-amino-2,4-dichloro-3-methylphenol;hydron;chloride Chemical compound Cl.CC1=C(Cl)C=C(N)C(O)=C1Cl ZOQYQHLEDJOHOK-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 abstract 1
- 238000004061 bleaching Methods 0.000 abstract 1
- 238000010531 catalytic reduction reaction Methods 0.000 abstract 1
- JIQJOKSCSVMZAN-UHFFFAOYSA-N ethyl 2-bromooctanoate Chemical compound CCCCCCC(Br)C(=O)OCC JIQJOKSCSVMZAN-UHFFFAOYSA-N 0.000 abstract 1
- KRAHENMBSVAAHD-UHFFFAOYSA-N ethyl 3-(4-methoxyphenyl)-3-oxopropanoate Chemical compound CCOC(=O)CC(=O)C1=CC=C(OC)C=C1 KRAHENMBSVAAHD-UHFFFAOYSA-N 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 150000002828 nitro derivatives Chemical class 0.000 abstract 1
- LQNUZADURLCDLV-IDEBNGHGSA-N nitrobenzene Chemical compound [O-][N+](=O)[13C]1=[13CH][13CH]=[13CH][13CH]=[13CH]1 LQNUZADURLCDLV-IDEBNGHGSA-N 0.000 abstract 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 abstract 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000001632 sodium acetate Substances 0.000 abstract 1
- 235000017281 sodium acetate Nutrition 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 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
- G03C7/3212—Couplers characterised by a group not in coupling site, e.g. ballast group, as far as the coupling rest is not specific
Landscapes
- 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 |
|---|---|---|---|
| DE2039489A DE2039489C3 (de) | 1970-08-08 | 1970-08-08 | Farbfotografisches Aufzeichnungsmaterial |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1356175A true GB1356175A (en) | 1974-06-12 |
Family
ID=5779224
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3693071A Expired GB1356175A (en) | 1970-08-08 | 1971-08-05 | Colour photogrphic silver halide material |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3770445A (enrdf_load_stackoverflow) |
| BE (1) | BE770812A (enrdf_load_stackoverflow) |
| CA (1) | CA969412A (enrdf_load_stackoverflow) |
| CH (1) | CH571237A5 (enrdf_load_stackoverflow) |
| DE (1) | DE2039489C3 (enrdf_load_stackoverflow) |
| FR (1) | FR2104077A5 (enrdf_load_stackoverflow) |
| GB (1) | GB1356175A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007536311A (ja) * | 2004-05-04 | 2007-12-13 | ノバルティス アクチエンゲゼルシャフト | Crth2受容体アンタゴニスト |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3941601A (en) * | 1972-03-23 | 1976-03-02 | Agfa-Gevaert, A.G. | Photographic silver halide material which contains color couplers |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2920961A (en) * | 1957-07-29 | 1960-01-12 | Eastman Kodak Co | Couplers for color photography |
| DE1127714B (de) * | 1960-08-20 | 1962-04-12 | Perutz Photowerke G M B H | Verfahren zur Herstellung von farbphotographischen Halogensilberemulsionen |
| GB1149514A (en) * | 1965-10-12 | 1969-04-23 | Fuji Photo Film Co Ltd | Colour couplers soluble in organic solvents and having an oil-solubilizing group |
-
1970
- 1970-08-08 DE DE2039489A patent/DE2039489C3/de not_active Expired
-
1971
- 1971-08-02 BE BE770812A patent/BE770812A/nl unknown
- 1971-08-03 CA CA119,634A patent/CA969412A/en not_active Expired
- 1971-08-04 US US00169146A patent/US3770445A/en not_active Expired - Lifetime
- 1971-08-05 CH CH1156071A patent/CH571237A5/xx not_active IP Right Cessation
- 1971-08-05 GB GB3693071A patent/GB1356175A/en not_active Expired
- 1971-08-06 FR FR7128957A patent/FR2104077A5/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007536311A (ja) * | 2004-05-04 | 2007-12-13 | ノバルティス アクチエンゲゼルシャフト | Crth2受容体アンタゴニスト |
Also Published As
| Publication number | Publication date |
|---|---|
| BE770812A (nl) | 1972-02-02 |
| FR2104077A5 (enrdf_load_stackoverflow) | 1972-04-14 |
| DE2039489A1 (de) | 1972-02-10 |
| CH571237A5 (enrdf_load_stackoverflow) | 1975-12-31 |
| DE2039489B2 (de) | 1978-12-07 |
| DE2039489C3 (de) | 1979-08-09 |
| US3770445A (en) | 1973-11-06 |
| CA969412A (en) | 1975-06-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |