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US4133955A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the production of 2-equivalent yellow couplers

Assignee: Agfa Gevaert AG
•
Filing: 1976-10-06
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Granted: 1979-01-09
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Expires: 1996-10-06
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Abstract

Abstract A one-stage process for the production of a 2-equivalent acylacetamide yellow coupler, in which one hydrogen atom of the α-methylene group of the acyl acetamide coupler molecule is substituted by a group which is attached through an oxygen or nitrogen atom and which can be split off during chromogenic development with an oxidized color developer containing a primary aromatic amino group, which process is carried out by reacting A 4-equivalent acylacetamide yellow coupler with A compound containing an aromatic hydroxyl group or an --NH-- group in a heterocyclic ring In the presence of a halogen, or an agent which releases halogen, and A basic condensation agent In a substantially aprotic solvent.

Inventors

  • 👤 Gunter Renner

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 11:10
CPC Classifications
G; G03; G03C; G03C7/00; G03C7/30; G03C7/305; G03C7/30511; G03C7/30517; G03C7/30535; C; C07; C07D; C07D239/00; C07D239/70; C07D239/72; C07D239/86; C07D239/88; C07D253/00; C07D253/08

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 117 words
In the process of converting a photographic 4-equivalent acyl acetamide yellow coupler to a 2-equivalent yellow coupler by a treatment that includes a reaction with a splittable-group-containing compound under basic condensation conditions that cause the active methylene carbon of the acyl acetamide to be substituted with a phenoxy or a heterocyclic ##STR6## which will split off during chromogenic photographic development, the improvement according to which the conversion to a 2-equivalent coupler is effected in a single reaction stage by reacting the 4-equivalent coupler in a substantially aprotic solvent with the splittable-group-containing compound, and a halogen under the basic condensation conditions to cause the splittable group to substitute directly on the active methylene of the 4 -equivalent coupler.
Claim 2
Dependent Claim 117 words
In the process of converting a photographic 4-equivalent acyl acetamide yellow coupler to a 2-equivalent yellow coupler by a treatment that includes a reaction with a splittable-group-containing compound under basic condensation conditions that cause the active methylene carbon of the acyl acetamide to be substituted with a phenoxy or a heterocyclic ##STR6## which will split off during chromogenic photographic development, the improvement according to which the conversion to a 2-equivalent coupler is effected in a single reaction stage by reacting the 4-equivalent coupler in a substantially aprotic solvent with the splittable-group-containing compound, and a halogen under the basic condensation conditions to cause the splittable group to substitute directly on the active methylene of the 4 -equivalent coupler.
Claim 3
Dependent Claim 13 words
The combination of claim 1 in which the halogen is bromine or iodine.
Claim 4
Dependent Claim 13 words
The combination of claim 1 in which the halogen is formed in situ.
Claim 5
Dependent Claim 28 words
The combination of claim 3 in which the halogen is formed by the interaction of a halide with an oxidizing agent that liberates the halogen from the halide.
Claim 6
Dependent Claim 21 words
The combination of claim 1 in which the reaction is effected at a temperature of from -20° C. to +100° C.
Claim 7
Dependent Claim 20 words
The combination of claim 2 in which the reaction is effected at a temperature from +5° C. to +20° C.
Claim 8
Dependent Claim 14 words
The combination of claim 1 in which the solvent is substantially a polar solvent.
Claim 9
Dependent Claim 24 words
The combination of claim 1 in which the splittable-group containing compound is a phenol substituted in paraposition by an acyl, carbamyl or sulfamyl radical.
Claim 10
Dependent Claim 32 words
The combination of claim 1 in which the splittable-group-containing compound has a 5- or 6-membered heterocyclic ring of carbon and nitrogen atoms with an NH adjacent to a ##STR7## or --CO-- structure.

References Cited (Backward Citations)

US3617291A Cited
US4057432A Cited
US3933500A Cited
US3928040A Cited
US4049458A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-01-08 1982-07-10 1983-01-09 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-01-08 1986-07-10 1987-01-09 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-01-08 1990-07-10 1991-01-09 $7700.00 Window Closed / Lapsed

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