Method for producing a color print comprising developing a specific material without benzyl alcohol

Claim 1

A process for producing a color print which comprises a steps of imagewise exposing to light a silver halide photosensitive material and then subjecting the exposed silver halide material to color development with a color developer containing benzyl alcohol in an amount less than or equal to 5 ml/l, the silver halide photosensitive material containing a reflecting support having provided thereon a red sensitive silver chlorobromide emulsion layer containing silver bromide in an amount of 10 mol % or less and at least one of the couplers represented by the following general formula (I) and the couplers represented by the following general formula (II), a green sensitive silver chlorobromide emulsion layer containing silver bromide in an amount of 10 mol % or less and at least one of the couplers represented by the following general formula (III), and a blue sensitive silver chlorobromide emulsion layer containing silver bromide in an amount of 10 mol % or less at least one of the couplers represented by the following general formula (IV); these couplers respectively existing in droplets of a high boiling organic solvent and/or water insoluble high molecular compound each having a dielectric constant of 2 to 20° at 25° C. and a refractive index of 1.3 to 1.7 at 25° C., said couplers being dispersed in the respective emulsion layers, and the spectral absorption peak wave lengths of the respective colored dyes as formed by coupling reaction of the respective couplers with the oxidized form of a paraphenylenediamine developing agent lying in the range represented by the following formula (I): 1/2(λy+λc)≧1/2(λy+λc)-10 (I) wherein λc=Spectral absorption peak wave length (nm) of the colored cyan dye λm=Spectral absorption peak wave length (nm) of the colored magenta dye λy=Spectral absorption peak wave length (nm) of the colored yellow dye ##STR21## wherein R 1 , R 2 and R 4 independently represent substituted or unsubstituted aliphatic, aromatic or heterocyclic groups; R 3 , R 5 and R 6 independently represent hydrogen atoms, halogen atoms, substituted or unsubstituted, aliphatic, aromatic groups or acylamino groups, and R 3 may represent with R 2 a nonmetal atomic group which forms a nitrogen-containing 5- or 6-membered ring; R 7 represents a hydrogen atom or a substituent; R 8 represents a substituted or unsubstituted N-phenylcarbamoyl group; Z a and Z b independently represent methines, substituted methines, ═N═ or --NH--; n is 0 or 1; and Y 1 , Y 2 , Y 3 and Y 4 independently represent hydrogen atoms or groups eliminable at the coupling reaction with the oxidized form of the developing agent.